Canonical Allele Identifier: CA2639241425

Gene: ACE

Linked Data

• gnomAD v4: 17-63483349-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63483350_63483351del , CM000679.2:g.63483350_63483351del	GRCh38
NC_000017.10:g.61560711_61560712del , CM000679.1:g.61560711_61560712del	GRCh37
NC_000017.9:g.58914443_58914444del	NCBI36
NG_011648.1:g.11278_11279del

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1488-110_1488-109del MANE Select	ENSP00000290866.4:n.1488-110_1488-109del
ENST00000290866.9:c.1488-110_1488-109del	ENSP00000290866.4:n.1488-110_1488-109del
ENST00000428043.5:c.1488-110_1488-109del	ENSP00000397593.2:n.1488-110_1488-109del
ENST00000582678.5:c.*887-110_*887-109del	ENSP00000462995.1:n.*887-110_*887-109del
ENST00000584529.5:n.1377-110_1377-109del
NM_000789.3:c.1488-110_1488-109del	NP_000780.1:n.1488-110_1488-109del
XM_005257110.1:c.939-110_939-109del	XP_005257167.1:n.939-110_939-109del
NM_000789.4:c.1488-110_1488-109del MANE Select	NP_000780.1:n.1488-110_1488-109del
NM_001382700.1:c.921-110_921-109del	NP_001369629.1:n.921-110_921-109del
NM_001382701.1:c.636-110_636-109del	NP_001369630.1:n.636-110_636-109del