Canonical Allele Identifier: CA2269940253

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477996T= , CM000679.2:g.63477996T=	GRCh38
NC_000017.10:g.61555357T= , CM000679.1:g.61555357T=	GRCh37
NC_000017.9:g.58909089T=	NCBI36
NG_011648.1:g.5924T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.315T= MANE Select	ENSP00000290866.4:p.Tyr105=
ENST00000290866.9:c.315T=	ENSP00000290866.4:p.Tyr105=
ENST00000428043.5:c.315T=	ENSP00000397593.2:p.Tyr105=
ENST00000579462.1:n.340T=
ENST00000580318.1:n.504T=
ENST00000582627.1:c.315T=	ENSP00000462280.1:p.Tyr105=
ENST00000582678.5:c.315T=	ENSP00000462995.1:p.Tyr105=
ENST00000583336.5:n.349T=
ENST00000584529.5:n.349T=
NM_000789.3:c.315T=	NP_000780.1:p.Tyr105=
XM_005257110.1:c.-141T=	XP_005257167.1:n.-141T=
NM_000789.4:c.315T= MANE Select	NP_000780.1:p.Tyr105=
NM_001382700.1:c.80T=	NP_001369629.1:p.Met27=
NM_001382701.1:c.-300T=	NP_001369630.1:n.-300T=