Canonical Allele Identifier: CA501341321

Gene: ACE

Linked Data

• dbSNP Id: rs1371697204
• gnomAD v3: 17-63477160-G-A
• gnomAD v4: 17-63477160-G-A
• MyVariant Identifiers: chr17:g.61554521G>A (hg19) ; chr17:g.63477160G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477160G>A , CM000679.2:g.63477160G>A	GRCh38
NC_000017.10:g.61554521G>A , CM000679.1:g.61554521G>A	GRCh37
NC_000017.9:g.58908253G>A	NCBI36
NG_011648.1:g.5088G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.66G>A MANE Select	ENSP00000290866.4:p.Leu22=
ENST00000290866.9:c.66G>A	ENSP00000290866.4:p.Leu22=
ENST00000428043.5:c.66G>A	ENSP00000397593.2:p.Leu22=
ENST00000579462.1:n.91G>A
ENST00000582678.5:c.66G>A	ENSP00000462995.1:p.Leu22=
ENST00000583336.5:n.100G>A
ENST00000584529.5:n.100G>A
NM_000789.3:c.66G>A	NP_000780.1:p.Leu22=
XM_005257110.1:c.-390G>A	XP_005257167.1:n.-390G>A
NM_000789.4:c.66G>A MANE Select	NP_000780.1:p.Leu22=
NM_001382700.1:c.-170G>A	NP_001369629.1:n.-170G>A
NM_001382701.1:c.-549G>A	NP_001369630.1:n.-549G>A