Canonical Allele Identifier: CA292874179

Gene: ACE

Linked Data

• dbSNP Id: rs757157948
• MyVariant Identifiers: chr17:g.61558138C>G (hg19) ; chr17:g.63480777C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63480777C>G , CM000679.2:g.63480777C>G	GRCh38
NC_000017.10:g.61558138C>G , CM000679.1:g.61558138C>G	GRCh37
NC_000017.9:g.58911870C>G	NCBI36
NG_011648.1:g.8705C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.847+249C>G MANE Select	ENSP00000290866.4:n.847+249C>G
ENST00000290866.9:c.847+249C>G	ENSP00000290866.4:n.847+249C>G
ENST00000428043.5:c.847+249C>G	ENSP00000397593.2:n.847+249C>G
ENST00000582627.1:c.847+249C>G	ENSP00000462280.1:n.847+249C>G
ENST00000582678.5:c.*246+249C>G	ENSP00000462995.1:n.*246+249C>G
ENST00000584529.5:n.881+249C>G
NM_000789.3:c.847+249C>G	NP_000780.1:n.847+249C>G
XM_005257110.1:c.298+249C>G	XP_005257167.1:n.298+249C>G
NM_000789.4:c.847+249C>G MANE Select	NP_000780.1:n.847+249C>G
NM_001382700.1:c.374+249C>G	NP_001369629.1:n.374+249C>G
NM_001382701.1:c.-6+249C>G	NP_001369630.1:n.-6+249C>G