Canonical Allele Identifier: CA773974882

Gene: ACE

Linked Data

• dbSNP Id: rs1224688383
• gnomAD v3: 17-63498026-G-A
• gnomAD v4: 17-63498026-G-A
• MyVariant Identifiers: chr17:g.61575387G>A (hg19) ; chr17:g.63498026G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498026G>A , CM000679.2:g.63498026G>A	GRCh38
NC_000017.10:g.61575387G>A , CM000679.1:g.61575387G>A	GRCh37
NC_000017.9:g.58929119G>A	NCBI36
NG_011648.1:g.25954G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.*660G>A MANE Select	ENSP00000290866.4:n.*660G>A
ENST00000290866.9:c.*660G>A	ENSP00000290866.4:n.*660G>A
ENST00000428043.5:c.*1003G>A	ENSP00000397593.2:n.*1003G>A
ENST00000577647.2:c.1969+1041G>A	ENSP00000464149.1:n.1969+1041G>A
NM_000789.3:c.*660G>A	NP_000780.1:n.*660G>A
NM_001178057.1:c.*660G>A	NP_001171528.1:n.*660G>A
NM_152830.2:c.*660G>A	NP_690043.1:n.*660G>A
XM_005257110.1:c.*660G>A	XP_005257167.1:n.*660G>A
XM_006721737.2:c.*660G>A	XP_006721800.2:n.*660G>A
NM_000789.4:c.*660G>A MANE Select	NP_000780.1:n.*660G>A
NM_001178057.2:c.*660G>A	NP_001171528.1:n.*660G>A
NM_152830.3:c.*660G>A	NP_690043.1:n.*660G>A
NM_001382700.1:c.*660G>A	NP_001369629.1:n.*660G>A
NM_001382701.1:c.*660G>A	NP_001369630.1:n.*660G>A
NM_001382702.1:c.*660G>A	NP_001369631.1:n.*660G>A
NR_168483.1:n.2959G>A