Canonical Allele Identifier: CA375249565
Community Standard Title: NM_005157.6(ABL1):c.1013T>A (p.Val338Glu)
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872965T>A , CM000671.2:g.130872965T>A GRCh38
NC_000009.11:g.133748352T>A , CM000671.1:g.133748352T>A GRCh37
NC_000009.10:g.132738173T>A NCBI36
NG_012034.1:g.164085T>A

Transcript Alleles

HGVS Amino-acid Change
NM_005157.6:c.1013T>A MANE Select NP_005148.2:p.Val338Glu
ENST00000318560.6:c.1013T>A MANE Select ENSP00000323315.5:p.Val338Glu
NM_005157.5:c.1013T>A NP_005148.2:p.Val338Glu
NM_007313.2:c.1070T>A NP_009297.2:p.Val357Glu
NM_007313.3:c.1070T>A NP_009297.2:p.Val357Glu
ENST00000318560.5:c.1013T>A ENSP00000323315.5:p.Val338Glu
ENST00000372348.6:c.1070T>A ENSP00000361423.2:p.Val357Glu
ENST00000372348.7:c.1070T>A ENSP00000361423.2:p.Val357Glu
ENST00000372348.9:c.1070T>A ENSP00000361423.2:p.Val357Glu