Allele Registry

HGVS	Genome Assembly
NC_000010.11:g.87863421_87863431delinsCCCCTGCCCTG , CM000672.2:g.87863421_87863431delinsCCCCTGCCCTG	GRCh38
NC_000010.10:g.89623178_89623188delinsCCCCTGCCCTG , CM000672.1:g.89623178_89623188delinsCCCCTGCCCTG	GRCh37
NC_000010.9:g.89613158_89613168delinsCCCCTGCCCTG	NCBI36
NG_007466.2:g.4984_4994delinsCCCCTGCCCTG , LRG_311:g.4984_4994delinsCCCCTGCCCTG
NG_033079.1:g.5007_5017delinsCAGGGCAGGGG

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+779_-17+789delinsCCCCTGCCCTG (PTEN)	ENSP00000516674.1:n.-17+779_-17+789delinsCCCCTGCCCTG
ENST00000688308.1:c.-17+308_-17+318delinsCCCCTGCCCTG (PTEN)	ENSP00000508752.1:n.-17+308_-17+318delinsCCCCTGCCCTG
ENST00000445946.5:c.-944_-934delinsCAGGGCAGGGG (KLLN) MANE Select	ENSP00000392204.2:n.-944_-934delinsCAGGGCAGGGG
ENST00000371953.7:c.-1049_-1039delinsCCCCTGCCCTG (PTEN)	ENSP00000361021.3:n.-1049_-1039delinsCCCCTGCCCTG
ENST00000445946.3:c.-944_-934delinsCAGGGCAGGGG (KLLN)	ENSP00000392204.2:n.-944_-934delinsCAGGGCAGGGG
NM_001126049.1:c.-944_-934delinsCAGGGCAGGGG (KLLN)	NP_001119521.1:n.-944_-934delinsCAGGGCAGGGG
NM_001126049.2:c.-944_-934delinsCAGGGCAGGGG (KLLN) MANE Select	NP_001119521.1:n.-944_-934delinsCAGGGCAGGGG