Canonical Allele Identifier: CA8698936

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477139G>C , CM000679.2:g.63477139G>C	GRCh38
NC_000017.10:g.61554500G>C , CM000679.1:g.61554500G>C	GRCh37
NC_000017.9:g.58908232G>C	NCBI36
NG_011648.1:g.5067G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.45G>C MANE Select	ENSP00000290866.4:p.Pro15=
ENST00000290866.9:c.45G>C	ENSP00000290866.4:p.Pro15=
ENST00000428043.5:c.45G>C	ENSP00000397593.2:p.Pro15=
ENST00000579462.1:n.70G>C
ENST00000582678.5:c.45G>C	ENSP00000462995.1:p.Pro15=
ENST00000583336.5:n.79G>C
ENST00000584529.5:n.79G>C
NM_000789.3:c.45G>C	NP_000780.1:p.Pro15=
XM_005257110.1:c.-411G>C	XP_005257167.1:n.-411G>C
NM_000789.4:c.45G>C MANE Select	NP_000780.1:p.Pro15=
NM_001382700.1:c.-191G>C	NP_001369629.1:n.-191G>C
NM_001382701.1:c.-570G>C	NP_001369630.1:n.-570G>C