Canonical Allele Identifier: CA400538480

Gene: ACE

Linked Data

• gnomAD v4: 17-63477161-C-A
• MyVariant Identifiers: chr17:g.61554522C>A (hg19) ; chr17:g.63477161C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477161C>A , CM000679.2:g.63477161C>A	GRCh38
NC_000017.10:g.61554522C>A , CM000679.1:g.61554522C>A	GRCh37
NC_000017.9:g.58908254C>A	NCBI36
NG_011648.1:g.5089C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.67C>A MANE Select	ENSP00000290866.4:p.Pro23Thr
ENST00000290866.9:c.67C>A	ENSP00000290866.4:p.Pro23Thr
ENST00000428043.5:c.67C>A	ENSP00000397593.2:p.Pro23Thr
ENST00000579462.1:n.92C>A
ENST00000582678.5:c.67C>A	ENSP00000462995.1:p.Pro23Thr
ENST00000583336.5:n.101C>A
ENST00000584529.5:n.101C>A
NM_000789.3:c.67C>A	NP_000780.1:p.Pro23Thr
XM_005257110.1:c.-389C>A	XP_005257167.1:n.-389C>A
NM_000789.4:c.67C>A MANE Select	NP_000780.1:p.Pro23Thr
NM_001382700.1:c.-169C>A	NP_001369629.1:n.-169C>A
NM_001382701.1:c.-548C>A	NP_001369630.1:n.-548C>A