Canonical Allele Identifier: CA400539500

Gene: ACE

Linked Data

• gnomAD v4: 17-63477612-C-T
• MyVariant Identifiers: chr17:g.61554973C>T (hg19) ; chr17:g.63477612C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477612C>T , CM000679.2:g.63477612C>T	GRCh38
NC_000017.10:g.61554973C>T , CM000679.1:g.61554973C>T	GRCh37
NC_000017.9:g.58908705C>T	NCBI36
NG_011648.1:g.5540C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.249+269C>T MANE Select	ENSP00000290866.4:n.249+269C>T
ENST00000290866.9:c.249+269C>T	ENSP00000290866.4:n.249+269C>T
ENST00000428043.5:c.249+269C>T	ENSP00000397593.2:n.249+269C>T
ENST00000579462.1:n.274+269C>T
ENST00000580318.1:n.120C>T
ENST00000582627.1:c.71C>T	ENSP00000462280.1:p.Pro24Leu
ENST00000582678.5:c.249+269C>T	ENSP00000462995.1:n.249+269C>T
ENST00000583336.5:n.283+269C>T
ENST00000584529.5:n.283+269C>T
NM_000789.3:c.249+269C>T	NP_000780.1:n.249+269C>T
XM_005257110.1:c.-207+269C>T	XP_005257167.1:n.-207+269C>T
NM_000789.4:c.249+269C>T MANE Select	NP_000780.1:n.249+269C>T
NM_001382700.1:c.14+269C>T	NP_001369629.1:n.14+269C>T
NM_001382701.1:c.-366+269C>T	NP_001369630.1:n.-366+269C>T