Canonical Allele Identifier: CA2639263208

Gene: ACE

Linked Data

• gnomAD v4: 17-63486814-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486814T>C , CM000679.2:g.63486814T>C	GRCh38
NC_000017.10:g.61564175T>C , CM000679.1:g.61564175T>C	GRCh37
NC_000017.9:g.58917907T>C	NCBI36
NG_011648.1:g.14742T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2217+99T>C MANE Select	ENSP00000290866.4:n.2217+99T>C
ENST00000290863.10:c.495+99T>C	ENSP00000290863.6:n.495+99T>C
ENST00000290866.9:c.2217+99T>C	ENSP00000290866.4:n.2217+99T>C
ENST00000413513.7:c.495+99T>C	ENSP00000392247.3:n.495+99T>C
ENST00000428043.5:c.2217+99T>C	ENSP00000397593.2:n.2217+99T>C
ENST00000577647.2:c.495+99T>C	ENSP00000464149.1:n.495+99T>C
ENST00000578839.5:c.*287+99T>C	ENSP00000462110.2:n.*287+99T>C
ENST00000579204.1:c.398+99T>C	ENSP00000464629.1:n.398+99T>C
ENST00000579314.5:c.495+99T>C	ENSP00000462599.1:n.495+99T>C
ENST00000579726.5:c.779+99T>C
ENST00000582005.5:c.*137+99T>C	ENSP00000462002.1:n.*137+99T>C
NM_000789.3:c.2217+99T>C	NP_000780.1:n.2217+99T>C
NM_001178057.1:c.495+99T>C	NP_001171528.1:n.495+99T>C
NM_152830.2:c.495+99T>C	NP_690043.1:n.495+99T>C
XM_005257110.1:c.1668+99T>C	XP_005257167.1:n.1668+99T>C
XM_006721737.2:c.555+99T>C	XP_006721800.2:n.555+99T>C
XM_006721737.3:c.555+99T>C	XP_006721800.2:n.555+99T>C
NM_000789.4:c.2217+99T>C MANE Select	NP_000780.1:n.2217+99T>C
NM_001178057.2:c.495+99T>C	NP_001171528.1:n.495+99T>C
NM_152830.3:c.495+99T>C	NP_690043.1:n.495+99T>C
NM_001382700.1:c.1650+99T>C	NP_001369629.1:n.1650+99T>C
NM_001382701.1:c.1365+99T>C	NP_001369630.1:n.1365+99T>C
NM_001382702.1:c.147+99T>C	NP_001369631.1:n.147+99T>C
NR_168483.1:n.517+99T>C