Canonical Allele Identifier: CA400539551

Gene: ACE

Linked Data

• gnomAD v4: 17-63477626-A-C
• MyVariant Identifiers: chr17:g.61554987A>C (hg19) ; chr17:g.63477626A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477626A>C , CM000679.2:g.63477626A>C	GRCh38
NC_000017.10:g.61554987A>C , CM000679.1:g.61554987A>C	GRCh37
NC_000017.9:g.58908719A>C	NCBI36
NG_011648.1:g.5554A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.249+283A>C MANE Select	ENSP00000290866.4:n.249+283A>C
ENST00000290866.9:c.249+283A>C	ENSP00000290866.4:n.249+283A>C
ENST00000428043.5:c.249+283A>C	ENSP00000397593.2:n.249+283A>C
ENST00000579462.1:n.274+283A>C
ENST00000580318.1:n.134A>C
ENST00000582627.1:c.85A>C	ENSP00000462280.1:p.Ser29Arg
ENST00000582678.5:c.249+283A>C	ENSP00000462995.1:n.249+283A>C
ENST00000583336.5:n.283+283A>C
ENST00000584529.5:n.283+283A>C
NM_000789.3:c.249+283A>C	NP_000780.1:n.249+283A>C
XM_005257110.1:c.-207+283A>C	XP_005257167.1:n.-207+283A>C
NM_000789.4:c.249+283A>C MANE Select	NP_000780.1:n.249+283A>C
NM_001382700.1:c.14+283A>C	NP_001369629.1:n.14+283A>C
NM_001382701.1:c.-366+283A>C	NP_001369630.1:n.-366+283A>C