Canonical Allele Identifier: CA8699118

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63479750C>G , CM000679.2:g.63479750C>G	GRCh38
NC_000017.10:g.61557111C>G , CM000679.1:g.61557111C>G	GRCh37
NC_000017.9:g.58910843C>G	NCBI36
NG_011648.1:g.7678C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.512-19C>G MANE Select	ENSP00000290866.4:n.512-19C>G
ENST00000290866.9:c.512-19C>G	ENSP00000290866.4:n.512-19C>G
ENST00000428043.5:c.512-19C>G	ENSP00000397593.2:n.512-19C>G
ENST00000580318.1:n.701-19C>G
ENST00000582627.1:c.512-19C>G	ENSP00000462280.1:n.512-19C>G
ENST00000582678.5:c.418-19C>G	ENSP00000462995.1:n.418-19C>G
ENST00000584529.5:n.546-19C>G
NM_000789.3:c.512-19C>G	NP_000780.1:n.512-19C>G
XM_005257110.1:c.-38-19C>G	XP_005257167.1:n.-38-19C>G
NM_000789.4:c.512-19C>G MANE Select	NP_000780.1:n.512-19C>G
NM_001382700.1:c.183-587C>G	NP_001369629.1:n.183-587C>G
NM_001382701.1:c.-197-587C>G	NP_001369630.1:n.-197-587C>G