Canonical Allele Identifier: CA400557823

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566026G>A (hg19) ; chr17:g.63488665G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488665G>A , CM000679.2:g.63488665G>A	GRCh38
NC_000017.10:g.61566026G>A , CM000679.1:g.61566026G>A	GRCh37
NC_000017.9:g.58919758G>A	NCBI36
NG_011648.1:g.16593G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2323G>A MANE Select	ENSP00000290866.4:p.Ala775Thr
ENST00000290863.10:c.601G>A	ENSP00000290863.6:p.Ala201Thr
ENST00000290866.9:c.2323G>A	ENSP00000290866.4:p.Ala775Thr
ENST00000413513.7:c.601G>A	ENSP00000392247.3:p.Ala201Thr
ENST00000428043.5:c.2323G>A	ENSP00000397593.2:p.Ala775Thr
ENST00000577647.2:c.601G>A	ENSP00000464149.1:p.Ala201Thr
ENST00000578839.5:c.*393G>A	ENSP00000462110.2:n.*393G>A
ENST00000579204.1:c.582G>A	ENSP00000464629.1:n.582G>A
ENST00000579314.5:c.*52G>A	ENSP00000462599.1:n.*52G>A
ENST00000582005.5:c.*243G>A	ENSP00000462002.1:n.*243G>A
ENST00000582761.1:c.91G>A	ENSP00000462909.1:p.Ala31Thr
ENST00000584865.5:n.269G>A
NM_000789.3:c.2323G>A	NP_000780.1:p.Ala775Thr
NM_001178057.1:c.601G>A	NP_001171528.1:p.Ala201Thr
NM_152830.2:c.601G>A	NP_690043.1:p.Ala201Thr
XM_005257110.1:c.1774G>A	XP_005257167.1:p.Ala592Thr
XM_006721737.2:c.661G>A	XP_006721800.2:p.Ala221Thr
XM_006721737.3:c.661G>A	XP_006721800.2:p.Ala221Thr
NM_000789.4:c.2323G>A MANE Select	NP_000780.1:p.Ala775Thr
NM_001178057.2:c.601G>A	NP_001171528.1:p.Ala201Thr
NM_152830.3:c.601G>A	NP_690043.1:p.Ala201Thr
NM_001382700.1:c.1756G>A	NP_001369629.1:p.Ala586Thr
NM_001382701.1:c.1471G>A	NP_001369630.1:p.Ala491Thr
NM_001382702.1:c.253G>A	NP_001369631.1:p.Ala85Thr
NR_168483.1:n.701G>A