Canonical Allele Identifier: CA400556787

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61564390C>A (hg19) ; chr17:g.63487029C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63487029C>A , CM000679.2:g.63487029C>A	GRCh38
NC_000017.10:g.61564390C>A , CM000679.1:g.61564390C>A	GRCh37
NC_000017.9:g.58918122C>A	NCBI36
NG_011648.1:g.14957C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2261C>A MANE Select	ENSP00000290866.4:p.Ala754Asp
ENST00000290863.10:c.539C>A	ENSP00000290863.6:p.Ala180Asp
ENST00000290866.9:c.2261C>A	ENSP00000290866.4:p.Ala754Asp
ENST00000413513.7:c.539C>A	ENSP00000392247.3:p.Ala180Asp
ENST00000428043.5:c.2261C>A	ENSP00000397593.2:p.Ala754Asp
ENST00000577647.2:c.539C>A	ENSP00000464149.1:p.Ala180Asp
ENST00000578839.5:c.*331C>A	ENSP00000462110.2:n.*331C>A
ENST00000579204.1:c.442C>A	ENSP00000464629.1:n.442C>A
ENST00000579314.5:c.539C>A	ENSP00000462599.1:p.Ala180Asp
ENST00000579726.5:c.823C>A
ENST00000582005.5:c.*181C>A	ENSP00000462002.1:n.*181C>A
ENST00000582761.1:c.29C>A	ENSP00000462909.1:p.Ala10Asp
ENST00000584865.5:n.207C>A
NM_000789.3:c.2261C>A	NP_000780.1:p.Ala754Asp
NM_001178057.1:c.539C>A	NP_001171528.1:p.Ala180Asp
NM_152830.2:c.539C>A	NP_690043.1:p.Ala180Asp
XM_005257110.1:c.1712C>A	XP_005257167.1:p.Ala571Asp
XM_006721737.2:c.599C>A	XP_006721800.2:p.Ala200Asp
XM_006721737.3:c.599C>A	XP_006721800.2:p.Ala200Asp
NM_000789.4:c.2261C>A MANE Select	NP_000780.1:p.Ala754Asp
NM_001178057.2:c.539C>A	NP_001171528.1:p.Ala180Asp
NM_152830.3:c.539C>A	NP_690043.1:p.Ala180Asp
NM_001382700.1:c.1694C>A	NP_001369629.1:p.Ala565Asp
NM_001382701.1:c.1409C>A	NP_001369630.1:p.Ala470Asp
NM_001382702.1:c.191C>A	NP_001369631.1:p.Ala64Asp
NR_168483.1:n.561C>A