Canonical Allele Identifier: CA400539850

Gene: ACE

Linked Data

• gnomAD v4: 17-63477669-G-T
• MyVariant Identifiers: chr17:g.61555030G>T (hg19) ; chr17:g.63477669G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477669G>T , CM000679.2:g.63477669G>T	GRCh38
NC_000017.10:g.61555030G>T , CM000679.1:g.61555030G>T	GRCh37
NC_000017.9:g.58908762G>T	NCBI36
NG_011648.1:g.5597G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.250-262G>T MANE Select	ENSP00000290866.4:n.250-262G>T
ENST00000290866.9:c.250-262G>T	ENSP00000290866.4:n.250-262G>T
ENST00000428043.5:c.250-262G>T	ENSP00000397593.2:n.250-262G>T
ENST00000579462.1:n.275-262G>T
ENST00000580318.1:n.177G>T
ENST00000582627.1:c.128G>T	ENSP00000462280.1:p.Arg43Leu
ENST00000582678.5:c.250-262G>T	ENSP00000462995.1:n.250-262G>T
ENST00000583336.5:n.284-262G>T
ENST00000584529.5:n.284-262G>T
NM_000789.3:c.250-262G>T	NP_000780.1:n.250-262G>T
XM_005257110.1:c.-206-262G>T	XP_005257167.1:n.-206-262G>T
NM_000789.4:c.250-262G>T MANE Select	NP_000780.1:n.250-262G>T
NM_001382700.1:c.15-262G>T	NP_001369629.1:n.15-262G>T
NM_001382701.1:c.-365-262G>T	NP_001369630.1:n.-365-262G>T