Canonical Allele Identifier: CA501182657

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61560821A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63483460A>C , CM000679.2:g.63483460A>C	GRCh38
NC_000017.10:g.61560821A>C , CM000679.1:g.61560821A>C	GRCh37
NC_000017.9:g.58914553A>C	NCBI36
NG_011648.1:g.11388A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1488A>C MANE Select	ENSP00000290866.4:p.Arg496=
ENST00000290866.9:c.1488A>C	ENSP00000290866.4:p.Arg496=
ENST00000428043.5:c.1488A>C	ENSP00000397593.2:p.Arg496=
ENST00000582678.5:c.*887A>C	ENSP00000462995.1:n.*887A>C
ENST00000584529.5:n.1377A>C
NM_000789.3:c.1488A>C	NP_000780.1:p.Arg496=
XM_005257110.1:c.939A>C	XP_005257167.1:p.Arg313=
NM_000789.4:c.1488A>C MANE Select	NP_000780.1:p.Arg496=
NM_001382700.1:c.921A>C	NP_001369629.1:p.Arg307=
NM_001382701.1:c.636A>C	NP_001369630.1:p.Arg212=