Canonical Allele Identifier: CA1941459998
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462072G= , CM000672.2:g.122462072G= GRCh38
NC_000010.10:g.124221588G= , CM000672.1:g.124221588G= GRCh37
NC_000010.9:g.124211578G= NCBI36
NG_011554.1:g.5548G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.420G= MANE Select ENSP00000357980.3:p.Glu140=
ENST00000648167.1:c.154+3363G= ENSP00000498033.1:n.154+3363G=
ENST00000368984.7:c.420G= ENSP00000357980.3:p.Glu140=
NM_002775.4:c.420G= NP_002766.1:p.Glu140=
NM_002775.5:c.420G= MANE Select NP_002766.1:p.Glu140=