Canonical Allele Identifier: CA773962857

Gene: ACE

Linked Data

• dbSNP Id: rs1427771332
• MyVariant Identifiers: chr17:g.61561138A>T (hg19) ; chr17:g.63483777A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63483777A>T , CM000679.2:g.63483777A>T	GRCh38
NC_000017.10:g.61561138A>T , CM000679.1:g.61561138A>T	GRCh37
NC_000017.9:g.58914870A>T	NCBI36
NG_011648.1:g.11705A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1587-72A>T MANE Select	ENSP00000290866.4:n.1587-72A>T
ENST00000290866.9:c.1587-72A>T	ENSP00000290866.4:n.1587-72A>T
ENST00000428043.5:c.1587-72A>T	ENSP00000397593.2:n.1587-72A>T
ENST00000582678.5:c.*986-72A>T	ENSP00000462995.1:n.*986-72A>T
NM_000789.3:c.1587-72A>T	NP_000780.1:n.1587-72A>T
XM_005257110.1:c.1038-72A>T	XP_005257167.1:n.1038-72A>T
NM_000789.4:c.1587-72A>T MANE Select	NP_000780.1:n.1587-72A>T
NM_001382700.1:c.1020-72A>T	NP_001369629.1:n.1020-72A>T
NM_001382701.1:c.735-72A>T	NP_001369630.1:n.735-72A>T