Canonical Allele Identifier: CA400567681

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61574313G>C (hg19) ; chr17:g.63496952G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496952G>C , CM000679.2:g.63496952G>C	GRCh38
NC_000017.10:g.61574313G>C , CM000679.1:g.61574313G>C	GRCh37
NC_000017.9:g.58928045G>C	NCBI36
NG_011648.1:g.24880G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3658G>C MANE Select	ENSP00000290866.4:p.Gly1220Arg
ENST00000290863.10:c.1936G>C	ENSP00000290863.6:p.Gly646Arg
ENST00000290866.9:c.3658G>C	ENSP00000290866.4:p.Gly1220Arg
ENST00000413513.7:c.1813G>C	ENSP00000392247.3:p.Gly605Arg
ENST00000428043.5:c.3658G>C	ENSP00000397593.2:p.Gly1220Arg
ENST00000577418.5:n.668G>C
ENST00000577647.2:c.1936G>C	ENSP00000464149.1:p.Gly646Arg
ENST00000578839.5:c.*1413G>C	ENSP00000462110.2:n.*1413G>C
ENST00000579314.5:c.*1387G>C	ENSP00000462599.1:n.*1387G>C
ENST00000579409.1:c.345G>C
ENST00000582244.1:n.532G>C
NM_000789.3:c.3658G>C	NP_000780.1:p.Gly1220Arg
NM_001178057.1:c.1813G>C	NP_001171528.1:p.Gly605Arg
NM_152830.2:c.1936G>C	NP_690043.1:p.Gly646Arg
XM_005257110.1:c.3109G>C	XP_005257167.1:p.Gly1037Arg
XM_006721737.2:c.1996G>C	XP_006721800.2:p.Gly666Arg
XM_006721737.3:c.1996G>C	XP_006721800.2:p.Gly666Arg
NM_000789.4:c.3658G>C MANE Select	NP_000780.1:p.Gly1220Arg
NM_001178057.2:c.1813G>C	NP_001171528.1:p.Gly605Arg
NM_152830.3:c.1936G>C	NP_690043.1:p.Gly646Arg
NM_001382700.1:c.3091G>C	NP_001369629.1:p.Gly1031Arg
NM_001382701.1:c.2806G>C	NP_001369630.1:p.Gly936Arg
NM_001382702.1:c.1273G>C	NP_001369631.1:p.Gly425Arg
NR_168483.1:n.2036G>C