Canonical Allele Identifier: CA292874271

Gene: ACE

Linked Data

• dbSNP Id: rs904972825
• gnomAD v3: 17-63480915-G-T
• gnomAD v4: 17-63480915-G-T
• MyVariant Identifiers: chr17:g.61558276G>T (hg19) ; chr17:g.63480915G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63480915G>T , CM000679.2:g.63480915G>T	GRCh38
NC_000017.10:g.61558276G>T , CM000679.1:g.61558276G>T	GRCh37
NC_000017.9:g.58912008G>T	NCBI36
NG_011648.1:g.8843G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.848-176G>T MANE Select	ENSP00000290866.4:n.848-176G>T
ENST00000290866.9:c.848-176G>T	ENSP00000290866.4:n.848-176G>T
ENST00000428043.5:c.848-176G>T	ENSP00000397593.2:n.848-176G>T
ENST00000582627.1:c.848-176G>T	ENSP00000462280.1:n.848-176G>T
ENST00000582678.5:c.*247-176G>T	ENSP00000462995.1:n.*247-176G>T
ENST00000584529.5:n.882-176G>T
NM_000789.3:c.848-176G>T	NP_000780.1:n.848-176G>T
XM_005257110.1:c.299-176G>T	XP_005257167.1:n.299-176G>T
NM_000789.4:c.848-176G>T MANE Select	NP_000780.1:n.848-176G>T
NM_001382700.1:c.375-176G>T	NP_001369629.1:n.375-176G>T
NM_001382701.1:c.-5-176G>T	NP_001369630.1:n.-5-176G>T