Canonical Allele Identifier: CA400549091

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61559867A>C (hg19) ; chr17:g.63482506A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482506A>C , CM000679.2:g.63482506A>C	GRCh38
NC_000017.10:g.61559867A>C , CM000679.1:g.61559867A>C	GRCh37
NC_000017.9:g.58913599A>C	NCBI36
NG_011648.1:g.10434A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1159A>C MANE Select	ENSP00000290866.4:p.Thr387Pro
ENST00000290866.9:c.1159A>C	ENSP00000290866.4:p.Thr387Pro
ENST00000428043.5:c.1159A>C	ENSP00000397593.2:p.Thr387Pro
ENST00000582678.5:c.*558A>C	ENSP00000462995.1:n.*558A>C
ENST00000584529.5:n.1193A>C
NM_000789.3:c.1159A>C	NP_000780.1:p.Thr387Pro
XM_005257110.1:c.610A>C	XP_005257167.1:p.Thr204Pro
NM_000789.4:c.1159A>C MANE Select	NP_000780.1:p.Thr387Pro
NM_001382700.1:c.592A>C	NP_001369629.1:p.Thr198Pro
NM_001382701.1:c.307A>C	NP_001369630.1:p.Thr103Pro