Canonical Allele Identifier: CA400556190

Gene: ACE

Linked Data

• dbSNP Id: rs1488331662
• gnomAD v2: 17-61564028-G-T
• gnomAD v4: 17-63486667-G-T
• MyVariant Identifiers: chr17:g.61564028G>T (hg19) ; chr17:g.63486667G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63486667G>T , CM000679.2:g.63486667G>T	GRCh38
NC_000017.10:g.61564028G>T , CM000679.1:g.61564028G>T	GRCh37
NC_000017.9:g.58917760G>T	NCBI36
NG_011648.1:g.14595G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2169G>T MANE Select	ENSP00000290866.4:p.Lys723Asn
ENST00000290863.10:c.447G>T	ENSP00000290863.6:p.Lys149Asn
ENST00000290866.9:c.2169G>T	ENSP00000290866.4:p.Lys723Asn
ENST00000413513.7:c.447G>T	ENSP00000392247.3:p.Lys149Asn
ENST00000428043.5:c.2169G>T	ENSP00000397593.2:p.Lys723Asn
ENST00000577647.2:c.447G>T	ENSP00000464149.1:p.Lys149Asn
ENST00000578839.5:c.*239G>T	ENSP00000462110.2:n.*239G>T
ENST00000579204.1:c.350G>T	ENSP00000464629.1:n.350G>T
ENST00000579314.5:c.447G>T	ENSP00000462599.1:p.Lys149Asn
ENST00000579726.5:c.731G>T
ENST00000582005.5:c.*89G>T	ENSP00000462002.1:n.*89G>T
NM_000789.3:c.2169G>T	NP_000780.1:p.Lys723Asn
NM_001178057.1:c.447G>T	NP_001171528.1:p.Lys149Asn
NM_152830.2:c.447G>T	NP_690043.1:p.Lys149Asn
XM_005257110.1:c.1620G>T	XP_005257167.1:p.Lys540Asn
XM_006721737.2:c.507G>T	XP_006721800.2:p.Lys169Asn
XM_006721737.3:c.507G>T	XP_006721800.2:p.Lys169Asn
NM_000789.4:c.2169G>T MANE Select	NP_000780.1:p.Lys723Asn
NM_001178057.2:c.447G>T	NP_001171528.1:p.Lys149Asn
NM_152830.3:c.447G>T	NP_690043.1:p.Lys149Asn
NM_001382700.1:c.1602G>T	NP_001369629.1:p.Lys534Asn
NM_001382701.1:c.1317G>T	NP_001369630.1:p.Lys439Asn
NM_001382702.1:c.99G>T	NP_001369631.1:p.Lys33Asn
NR_168483.1:n.469G>T