Canonical Allele Identifier: CA501341622

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61559851G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482490G>C , CM000679.2:g.63482490G>C	GRCh38
NC_000017.10:g.61559851G>C , CM000679.1:g.61559851G>C	GRCh37
NC_000017.9:g.58913583G>C	NCBI36
NG_011648.1:g.10418G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1143G>C MANE Select	ENSP00000290866.4:p.Thr381=
ENST00000290866.9:c.1143G>C	ENSP00000290866.4:p.Thr381=
ENST00000428043.5:c.1143G>C	ENSP00000397593.2:p.Thr381=
ENST00000582678.5:c.*542G>C	ENSP00000462995.1:n.*542G>C
ENST00000584529.5:n.1177G>C
NM_000789.3:c.1143G>C	NP_000780.1:p.Thr381=
XM_005257110.1:c.594G>C	XP_005257167.1:p.Thr198=
NM_000789.4:c.1143G>C MANE Select	NP_000780.1:p.Thr381=
NM_001382700.1:c.576G>C	NP_001369629.1:p.Thr192=
NM_001382701.1:c.291G>C	NP_001369630.1:p.Thr97=