Canonical Allele Identifier: CA400540723

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61555365T>C (hg19) ; chr17:g.63478004T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478004T>C , CM000679.2:g.63478004T>C	GRCh38
NC_000017.10:g.61555365T>C , CM000679.1:g.61555365T>C	GRCh37
NC_000017.9:g.58909097T>C	NCBI36
NG_011648.1:g.5932T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.323T>C MANE Select	ENSP00000290866.4:p.Ile108Thr
ENST00000290866.9:c.323T>C	ENSP00000290866.4:p.Ile108Thr
ENST00000428043.5:c.323T>C	ENSP00000397593.2:p.Ile108Thr
ENST00000579462.1:n.348T>C
ENST00000580318.1:n.512T>C
ENST00000582627.1:c.323T>C	ENSP00000462280.1:p.Ile108Thr
ENST00000582678.5:c.323T>C	ENSP00000462995.1:p.Ile108Thr
ENST00000583336.5:n.357T>C
ENST00000584529.5:n.357T>C
NM_000789.3:c.323T>C	NP_000780.1:p.Ile108Thr
XM_005257110.1:c.-133T>C	XP_005257167.1:n.-133T>C
NM_000789.4:c.323T>C MANE Select	NP_000780.1:p.Ile108Thr
NM_001382700.1:c.88T>C	NP_001369629.1:p.Ser30Pro
NM_001382701.1:c.-292T>C	NP_001369630.1:n.-292T>C