Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222541_7222547delinsGGCTGTA , CM000679.2:g.7222541_7222547delinsGGCTGTA	GRCh38
NC_000017.10:g.7125860_7125866delinsGGCTGTA , CM000679.1:g.7125860_7125866delinsGGCTGTA	GRCh37
NC_000017.9:g.7066584_7066590delinsGGCTGTA	NCBI36
NG_007975.1:g.7708_7714delinsGGCTGTA
NG_008391.2:g.2504_2510delinsTACAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.879-126_879-120delinsGGCTGTA MANE Select	ENSP00000349297.5:n.879-126_879-120delinsGGCTGTA
ENST00000322910.9:c.834-126_834-120delinsGGCTGTA	ENSP00000325395.5:n.834-126_834-120delinsGGCTGTA
ENST00000350303.9:c.813-126_813-120delinsGGCTGTA	ENSP00000344152.5:n.813-126_813-120delinsGGCTGTA
ENST00000356839.9:c.879-126_879-120delinsGGCTGTA	ENSP00000349297.5:n.879-126_879-120delinsGGCTGTA
ENST00000543245.6:c.948-126_948-120delinsGGCTGTA	ENSP00000438689.2:n.948-126_948-120delinsGGCTGTA
ENST00000581378.5:c.597-126_597-120delinsGGCTGTA
ENST00000582379.1:n.263-126_263-120delinsGGCTGTA
NM_000018.3:c.879-126_879-120delinsGGCTGTA	NP_000009.1:n.879-126_879-120delinsGGCTGTA
NM_001033859.2:c.813-126_813-120delinsGGCTGTA	NP_001029031.1:n.813-126_813-120delinsGGCTGTA
NM_001270447.1:c.948-126_948-120delinsGGCTGTA	NP_001257376.1:n.948-126_948-120delinsGGCTGTA
NM_001270448.1:c.651-126_651-120delinsGGCTGTA	NP_001257377.1:n.651-126_651-120delinsGGCTGTA
XM_006721516.2:c.879-126_879-120delinsGGCTGTA	XP_006721579.2:n.879-126_879-120delinsGGCTGTA
XM_011523829.1:c.879-126_879-120delinsGGCTGTA	XP_011522131.1:n.879-126_879-120delinsGGCTGTA
XM_011523830.1:c.879-126_879-120delinsGGCTGTA	XP_011522132.1:n.879-126_879-120delinsGGCTGTA
XR_934021.1:n.986-126_986-120delinsGGCTGTA
XR_934022.1:n.986-126_986-120delinsGGCTGTA
XR_934023.1:n.986-126_986-120delinsGGCTGTA
XM_006721516.3:c.879-126_879-120delinsGGCTGTA	XP_006721579.2:n.879-126_879-120delinsGGCTGTA
XM_011523829.2:c.879-126_879-120delinsGGCTGTA	XP_011522131.1:n.879-126_879-120delinsGGCTGTA
XM_011523830.2:c.879-126_879-120delinsGGCTGTA	XP_011522132.1:n.879-126_879-120delinsGGCTGTA
XM_024450741.1:c.879-126_879-120delinsGGCTGTA	XP_024306509.1:n.879-126_879-120delinsGGCTGTA
XR_934021.2:n.938-126_938-120delinsGGCTGTA
XR_934022.2:n.938-126_938-120delinsGGCTGTA
XR_934023.2:n.938-126_938-120delinsGGCTGTA
NM_000018.4:c.879-126_879-120delinsGGCTGTA MANE Select	NP_000009.1:n.879-126_879-120delinsGGCTGTA
NM_001033859.3:c.813-126_813-120delinsGGCTGTA	NP_001029031.1:n.813-126_813-120delinsGGCTGTA
NM_001270447.2:c.948-126_948-120delinsGGCTGTA	NP_001257376.1:n.948-126_948-120delinsGGCTGTA
NM_001270448.2:c.651-126_651-120delinsGGCTGTA	NP_001257377.1:n.651-126_651-120delinsGGCTGTA