Canonical Allele Identifier: CA2269941707

Gene: ACE

Linked Data

• dbSNP Id: rs2049695913

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63480874A>G , CM000679.2:g.63480874A>G	GRCh38
NC_000017.10:g.61558235A>G , CM000679.1:g.61558235A>G	GRCh37
NC_000017.9:g.58911967A>G	NCBI36
NG_011648.1:g.8802A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.848-217A>G MANE Select	ENSP00000290866.4:n.848-217A>G
ENST00000290866.9:c.848-217A>G	ENSP00000290866.4:n.848-217A>G
ENST00000428043.5:c.848-217A>G	ENSP00000397593.2:n.848-217A>G
ENST00000582627.1:c.848-217A>G	ENSP00000462280.1:n.848-217A>G
ENST00000582678.5:c.*247-217A>G	ENSP00000462995.1:n.*247-217A>G
ENST00000584529.5:n.882-217A>G
NM_000789.3:c.848-217A>G	NP_000780.1:n.848-217A>G
XM_005257110.1:c.299-217A>G	XP_005257167.1:n.299-217A>G
NM_000789.4:c.848-217A>G MANE Select	NP_000780.1:n.848-217A>G
NM_001382700.1:c.375-217A>G	NP_001369629.1:n.375-217A>G
NM_001382701.1:c.-5-217A>G	NP_001369630.1:n.-5-217A>G