Canonical Allele Identifier: CA2269945949

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488695T= , CM000679.2:g.63488695T=	GRCh38
NC_000017.10:g.61566056T= , CM000679.1:g.61566056T=	GRCh37
NC_000017.9:g.58919788T=	NCBI36
NG_011648.1:g.16623T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2353T= MANE Select	ENSP00000290866.4:p.Trp785=
ENST00000290863.10:c.631T=	ENSP00000290863.6:p.Trp211=
ENST00000290866.9:c.2353T=	ENSP00000290866.4:p.Trp785=
ENST00000413513.7:c.631T=	ENSP00000392247.3:p.Trp211=
ENST00000428043.5:c.2353T=	ENSP00000397593.2:p.Trp785=
ENST00000577647.2:c.631T=	ENSP00000464149.1:p.Trp211=
ENST00000578839.5:c.*423T=	ENSP00000462110.2:n.*423T=
ENST00000579204.1:c.612T=	ENSP00000464629.1:n.612T=
ENST00000579314.5:c.*82T=	ENSP00000462599.1:n.*82T=
ENST00000582005.5:c.*273T=	ENSP00000462002.1:n.*273T=
ENST00000582761.1:c.121T=	ENSP00000462909.1:p.Trp41=
ENST00000584865.5:n.299T=
NM_000789.3:c.2353T=	NP_000780.1:p.Trp785=
NM_001178057.1:c.631T=	NP_001171528.1:p.Trp211=
NM_152830.2:c.631T=	NP_690043.1:p.Trp211=
XM_005257110.1:c.1804T=	XP_005257167.1:p.Trp602=
XM_006721737.2:c.691T=	XP_006721800.2:p.Trp231=
XM_006721737.3:c.691T=	XP_006721800.2:p.Trp231=
NM_000789.4:c.2353T= MANE Select	NP_000780.1:p.Trp785=
NM_001178057.2:c.631T=	NP_001171528.1:p.Trp211=
NM_152830.3:c.631T=	NP_690043.1:p.Trp211=
NM_001382700.1:c.1786T=	NP_001369629.1:p.Trp596=
NM_001382701.1:c.1501T=	NP_001369630.1:p.Trp501=
NM_001382702.1:c.283T=	NP_001369631.1:p.Trp95=
NR_168483.1:n.731T=