Canonical Allele Identifier: CA292874254

Gene: ACE

Linked Data

• dbSNP Id: rs868218634
• MyVariant Identifiers: chr17:g.61558261G>A (hg19) ; chr17:g.63480900G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63480900G>A , CM000679.2:g.63480900G>A	GRCh38
NC_000017.10:g.61558261G>A , CM000679.1:g.61558261G>A	GRCh37
NC_000017.9:g.58911993G>A	NCBI36
NG_011648.1:g.8828G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.848-191G>A MANE Select	ENSP00000290866.4:n.848-191G>A
ENST00000290866.9:c.848-191G>A	ENSP00000290866.4:n.848-191G>A
ENST00000428043.5:c.848-191G>A	ENSP00000397593.2:n.848-191G>A
ENST00000582627.1:c.848-191G>A	ENSP00000462280.1:n.848-191G>A
ENST00000582678.5:c.*247-191G>A	ENSP00000462995.1:n.*247-191G>A
ENST00000584529.5:n.882-191G>A
NM_000789.3:c.848-191G>A	NP_000780.1:n.848-191G>A
XM_005257110.1:c.299-191G>A	XP_005257167.1:n.299-191G>A
NM_000789.4:c.848-191G>A MANE Select	NP_000780.1:n.848-191G>A
NM_001382700.1:c.375-191G>A	NP_001369629.1:n.375-191G>A
NM_001382701.1:c.-5-191G>A	NP_001369630.1:n.-5-191G>A