Canonical Allele Identifier: CA400540489

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61555153T>C (hg19) ; chr17:g.63477792T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477792T>C , CM000679.2:g.63477792T>C	GRCh38
NC_000017.10:g.61555153T>C , CM000679.1:g.61555153T>C	GRCh37
NC_000017.9:g.58908885T>C	NCBI36
NG_011648.1:g.5720T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.250-139T>C MANE Select	ENSP00000290866.4:n.250-139T>C
ENST00000290866.9:c.250-139T>C	ENSP00000290866.4:n.250-139T>C
ENST00000428043.5:c.250-139T>C	ENSP00000397593.2:n.250-139T>C
ENST00000579462.1:n.275-139T>C
ENST00000580318.1:n.300T>C
ENST00000582627.1:c.249+2T>C	ENSP00000462280.1:n.249+2T>C
ENST00000582678.5:c.250-139T>C	ENSP00000462995.1:n.250-139T>C
ENST00000583336.5:n.284-139T>C
ENST00000584529.5:n.284-139T>C
NM_000789.3:c.250-139T>C	NP_000780.1:n.250-139T>C
XM_005257110.1:c.-206-139T>C	XP_005257167.1:n.-206-139T>C
NM_000789.4:c.250-139T>C MANE Select	NP_000780.1:n.250-139T>C
NM_001382700.1:c.15-139T>C	NP_001369629.1:n.15-139T>C
NM_001382701.1:c.-365-139T>C	NP_001369630.1:n.-365-139T>C