Canonical Allele Identifier: CA400540742

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61555373A>C (hg19) ; chr17:g.63478012A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478012A>C , CM000679.2:g.63478012A>C	GRCh38
NC_000017.10:g.61555373A>C , CM000679.1:g.61555373A>C	GRCh37
NC_000017.9:g.58909105A>C	NCBI36
NG_011648.1:g.5940A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.331A>C MANE Select	ENSP00000290866.4:p.Asn111His
ENST00000290866.9:c.331A>C	ENSP00000290866.4:p.Asn111His
ENST00000428043.5:c.331A>C	ENSP00000397593.2:p.Asn111His
ENST00000579462.1:n.356A>C
ENST00000580318.1:n.520A>C
ENST00000582627.1:c.331A>C	ENSP00000462280.1:p.Asn111His
ENST00000582678.5:c.331A>C	ENSP00000462995.1:p.Asn111His
ENST00000583336.5:n.365A>C
ENST00000584529.5:n.365A>C
NM_000789.3:c.331A>C	NP_000780.1:p.Asn111His
XM_005257110.1:c.-125A>C	XP_005257167.1:n.-125A>C
NM_000789.4:c.331A>C MANE Select	NP_000780.1:p.Asn111His
NM_001382700.1:c.96A>C	NP_001369629.1:p.Arg32Ser
NM_001382701.1:c.-284A>C	NP_001369630.1:n.-284A>C