Canonical Allele Identifier: CA773962539

Gene: ACE

Linked Data

• dbSNP Id: rs1388903866
• MyVariant Identifiers: chr17:g.61560781A>C (hg19) ; chr17:g.63483420A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63483420A>C , CM000679.2:g.63483420A>C	GRCh38
NC_000017.10:g.61560781A>C , CM000679.1:g.61560781A>C	GRCh37
NC_000017.9:g.58914513A>C	NCBI36
NG_011648.1:g.11348A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1488-40A>C MANE Select	ENSP00000290866.4:n.1488-40A>C
ENST00000290866.9:c.1488-40A>C	ENSP00000290866.4:n.1488-40A>C
ENST00000428043.5:c.1488-40A>C	ENSP00000397593.2:n.1488-40A>C
ENST00000582678.5:c.*887-40A>C	ENSP00000462995.1:n.*887-40A>C
ENST00000584529.5:n.1377-40A>C
NM_000789.3:c.1488-40A>C	NP_000780.1:n.1488-40A>C
XM_005257110.1:c.939-40A>C	XP_005257167.1:n.939-40A>C
NM_000789.4:c.1488-40A>C MANE Select	NP_000780.1:n.1488-40A>C
NM_001382700.1:c.921-40A>C	NP_001369629.1:n.921-40A>C
NM_001382701.1:c.636-40A>C	NP_001369630.1:n.636-40A>C