Canonical Allele Identifier: CA8699621

Gene: ACE

Linked Data

• dbSNP Id: rs753923047
• ExAC: 17:61561163 T / C
• gnomAD v2: 17-61561163-T-C
• gnomAD v4: 17-63483802-T-C
• MyVariant Identifiers: chr17:g.61561163T>C (hg19) ; chr17:g.63483802T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63483802T>C , CM000679.2:g.63483802T>C	GRCh38
NC_000017.10:g.61561163T>C , CM000679.1:g.61561163T>C	GRCh37
NC_000017.9:g.58914895T>C	NCBI36
NG_011648.1:g.11730T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1587-47T>C MANE Select	ENSP00000290866.4:n.1587-47T>C
ENST00000290866.9:c.1587-47T>C	ENSP00000290866.4:n.1587-47T>C
ENST00000428043.5:c.1587-47T>C	ENSP00000397593.2:n.1587-47T>C
ENST00000582678.5:c.*986-47T>C	ENSP00000462995.1:n.*986-47T>C
NM_000789.3:c.1587-47T>C	NP_000780.1:n.1587-47T>C
XM_005257110.1:c.1038-47T>C	XP_005257167.1:n.1038-47T>C
NM_000789.4:c.1587-47T>C MANE Select	NP_000780.1:n.1587-47T>C
NM_001382700.1:c.1020-47T>C	NP_001369629.1:n.1020-47T>C
NM_001382701.1:c.735-47T>C	NP_001369630.1:n.735-47T>C