Canonical Allele Identifier: CA501342392

Gene: ACE

Linked Data

• gnomAD v4: 17-63496900-G-A
• MyVariant Identifiers: chr17:g.61574261G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496900G>A , CM000679.2:g.63496900G>A	GRCh38
NC_000017.10:g.61574261G>A , CM000679.1:g.61574261G>A	GRCh37
NC_000017.9:g.58927993G>A	NCBI36
NG_011648.1:g.24828G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.3606G>A MANE Select	ENSP00000290866.4:p.Lys1202=
ENST00000290863.10:c.1884G>A	ENSP00000290863.6:p.Lys628=
ENST00000290866.9:c.3606G>A	ENSP00000290866.4:p.Lys1202=
ENST00000413513.7:c.1761G>A	ENSP00000392247.3:p.Lys587=
ENST00000428043.5:c.3606G>A	ENSP00000397593.2:p.Lys1202=
ENST00000577418.5:n.616G>A
ENST00000577647.2:c.1884G>A	ENSP00000464149.1:p.Lys628=
ENST00000578839.5:c.*1361G>A	ENSP00000462110.2:n.*1361G>A
ENST00000579314.5:c.*1335G>A	ENSP00000462599.1:n.*1335G>A
ENST00000579409.1:c.293G>A
ENST00000582244.1:n.480G>A
NM_000789.3:c.3606G>A	NP_000780.1:p.Lys1202=
NM_001178057.1:c.1761G>A	NP_001171528.1:p.Lys587=
NM_152830.2:c.1884G>A	NP_690043.1:p.Lys628=
XM_005257110.1:c.3057G>A	XP_005257167.1:p.Lys1019=
XM_006721737.2:c.1944G>A	XP_006721800.2:p.Lys648=
XM_006721737.3:c.1944G>A	XP_006721800.2:p.Lys648=
NM_000789.4:c.3606G>A MANE Select	NP_000780.1:p.Lys1202=
NM_001178057.2:c.1761G>A	NP_001171528.1:p.Lys587=
NM_152830.3:c.1884G>A	NP_690043.1:p.Lys628=
NM_001382700.1:c.3039G>A	NP_001369629.1:p.Lys1013=
NM_001382701.1:c.2754G>A	NP_001369630.1:p.Lys918=
NM_001382702.1:c.1221G>A	NP_001369631.1:p.Lys407=
NR_168483.1:n.1984G>A