Canonical Allele Identifier: CA400539818

Gene: ACE

Linked Data

• gnomAD v4: 17-63477665-C-A
• MyVariant Identifiers: chr17:g.61555026C>A (hg19) ; chr17:g.63477665C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477665C>A , CM000679.2:g.63477665C>A	GRCh38
NC_000017.10:g.61555026C>A , CM000679.1:g.61555026C>A	GRCh37
NC_000017.9:g.58908758C>A	NCBI36
NG_011648.1:g.5593C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.250-266C>A MANE Select	ENSP00000290866.4:n.250-266C>A
ENST00000290866.9:c.250-266C>A	ENSP00000290866.4:n.250-266C>A
ENST00000428043.5:c.250-266C>A	ENSP00000397593.2:n.250-266C>A
ENST00000579462.1:n.275-266C>A
ENST00000580318.1:n.173C>A
ENST00000582627.1:c.124C>A	ENSP00000462280.1:p.His42Asn
ENST00000582678.5:c.250-266C>A	ENSP00000462995.1:n.250-266C>A
ENST00000583336.5:n.284-266C>A
ENST00000584529.5:n.284-266C>A
NM_000789.3:c.250-266C>A	NP_000780.1:n.250-266C>A
XM_005257110.1:c.-206-266C>A	XP_005257167.1:n.-206-266C>A
NM_000789.4:c.250-266C>A MANE Select	NP_000780.1:n.250-266C>A
NM_001382700.1:c.15-266C>A	NP_001369629.1:n.15-266C>A
NM_001382701.1:c.-365-266C>A	NP_001369630.1:n.-365-266C>A