Canonical Allele Identifier: CA400549596

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61559924G>C (hg19) ; chr17:g.63482563G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482563G>C , CM000679.2:g.63482563G>C	GRCh38
NC_000017.10:g.61559924G>C , CM000679.1:g.61559924G>C	GRCh37
NC_000017.9:g.58913656G>C	NCBI36
NG_011648.1:g.10491G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.1216G>C MANE Select	ENSP00000290866.4:p.Val406Leu
ENST00000290866.9:c.1216G>C	ENSP00000290866.4:p.Val406Leu
ENST00000428043.5:c.1216G>C	ENSP00000397593.2:p.Val406Leu
ENST00000582678.5:c.*615G>C	ENSP00000462995.1:n.*615G>C
ENST00000584529.5:n.1250G>C
NM_000789.3:c.1216G>C	NP_000780.1:p.Val406Leu
XM_005257110.1:c.667G>C	XP_005257167.1:p.Val223Leu
NM_000789.4:c.1216G>C MANE Select	NP_000780.1:p.Val406Leu
NM_001382700.1:c.649G>C	NP_001369629.1:p.Val217Leu
NM_001382701.1:c.364G>C	NP_001369630.1:p.Val122Leu