Canonical Allele Identifier: CA400549601

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61559925T>C (hg19) ; chr17:g.63482564T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482564T>C , CM000679.2:g.63482564T>C	GRCh38
NC_000017.10:g.61559925T>C , CM000679.1:g.61559925T>C	GRCh37
NC_000017.9:g.58913657T>C	NCBI36
NG_011648.1:g.10492T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1217T>C MANE Select	ENSP00000290866.4:p.Val406Ala
ENST00000290866.9:c.1217T>C	ENSP00000290866.4:p.Val406Ala
ENST00000428043.5:c.1217T>C	ENSP00000397593.2:p.Val406Ala
ENST00000582678.5:c.*616T>C	ENSP00000462995.1:n.*616T>C
ENST00000584529.5:n.1251T>C
NM_000789.3:c.1217T>C	NP_000780.1:p.Val406Ala
XM_005257110.1:c.668T>C	XP_005257167.1:p.Val223Ala
NM_000789.4:c.1217T>C MANE Select	NP_000780.1:p.Val406Ala
NM_001382700.1:c.650T>C	NP_001369629.1:p.Val217Ala
NM_001382701.1:c.365T>C	NP_001369630.1:p.Val122Ala