Canonical Allele Identifier: CA2269940029

Gene: ACE

Linked Data

• dbSNP Id: rs2049639270
• gnomAD v4: 17-63477577-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477577C>T , CM000679.2:g.63477577C>T	GRCh38
NC_000017.10:g.61554938C>T , CM000679.1:g.61554938C>T	GRCh37
NC_000017.9:g.58908670C>T	NCBI36
NG_011648.1:g.5505C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.249+234C>T MANE Select	ENSP00000290866.4:n.249+234C>T
ENST00000290866.9:c.249+234C>T	ENSP00000290866.4:n.249+234C>T
ENST00000428043.5:c.249+234C>T	ENSP00000397593.2:n.249+234C>T
ENST00000579462.1:n.274+234C>T
ENST00000580318.1:n.85C>T
ENST00000582627.1:c.36C>T	ENSP00000462280.1:p.Ala12=
ENST00000582678.5:c.249+234C>T	ENSP00000462995.1:n.249+234C>T
ENST00000583336.5:n.283+234C>T
ENST00000584529.5:n.283+234C>T
NM_000789.3:c.249+234C>T	NP_000780.1:n.249+234C>T
XM_005257110.1:c.-207+234C>T	XP_005257167.1:n.-207+234C>T
NM_000789.4:c.249+234C>T MANE Select	NP_000780.1:n.249+234C>T
NM_001382700.1:c.14+234C>T	NP_001369629.1:n.14+234C>T
NM_001382701.1:c.-366+234C>T	NP_001369630.1:n.-366+234C>T