Canonical Allele Identifier: CA400557891

Gene: ACE

Linked Data

• COSMIC: COSM397539
• MyVariant Identifiers: chr17:g.61566059G>A (hg19) ; chr17:g.63488698G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488698G>A , CM000679.2:g.63488698G>A	GRCh38
NC_000017.10:g.61566059G>A , CM000679.1:g.61566059G>A	GRCh37
NC_000017.9:g.58919791G>A	NCBI36
NG_011648.1:g.16626G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2356G>A MANE Select	ENSP00000290866.4:p.Ala786Thr
ENST00000290863.10:c.634G>A	ENSP00000290863.6:p.Ala212Thr
ENST00000290866.9:c.2356G>A	ENSP00000290866.4:p.Ala786Thr
ENST00000413513.7:c.634G>A	ENSP00000392247.3:p.Ala212Thr
ENST00000428043.5:c.2356G>A	ENSP00000397593.2:p.Ala786Thr
ENST00000577647.2:c.634G>A	ENSP00000464149.1:p.Ala212Thr
ENST00000578839.5:c.*426G>A	ENSP00000462110.2:n.*426G>A
ENST00000579204.1:c.615G>A	ENSP00000464629.1:n.615G>A
ENST00000579314.5:c.*85G>A	ENSP00000462599.1:n.*85G>A
ENST00000582005.5:c.*276G>A	ENSP00000462002.1:n.*276G>A
ENST00000582761.1:c.124G>A	ENSP00000462909.1:p.Ala42Thr
ENST00000584865.5:n.302G>A
NM_000789.3:c.2356G>A	NP_000780.1:p.Ala786Thr
NM_001178057.1:c.634G>A	NP_001171528.1:p.Ala212Thr
NM_152830.2:c.634G>A	NP_690043.1:p.Ala212Thr
XM_005257110.1:c.1807G>A	XP_005257167.1:p.Ala603Thr
XM_006721737.2:c.694G>A	XP_006721800.2:p.Ala232Thr
XM_006721737.3:c.694G>A	XP_006721800.2:p.Ala232Thr
NM_000789.4:c.2356G>A MANE Select	NP_000780.1:p.Ala786Thr
NM_001178057.2:c.634G>A	NP_001171528.1:p.Ala212Thr
NM_152830.3:c.634G>A	NP_690043.1:p.Ala212Thr
NM_001382700.1:c.1789G>A	NP_001369629.1:p.Ala597Thr
NM_001382701.1:c.1504G>A	NP_001369630.1:p.Ala502Thr
NM_001382702.1:c.286G>A	NP_001369631.1:p.Ala96Thr
NR_168483.1:n.734G>A