Canonical Allele Identifier: CA1941467391
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472099G= , CM000672.2:g.122472099G= GRCh38
NC_000010.10:g.124231615G= , CM000672.1:g.124231615G= GRCh37
NC_000010.9:g.124221605G= NCBI36
NG_011554.1:g.15575G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+9975G= MANE Select ENSP00000357980.3:n.472+9975G=
ENST00000648167.1:c.154+13390G= ENSP00000498033.1:n.154+13390G=
ENST00000368984.7:c.472+9975G= ENSP00000357980.3:n.472+9975G=
NM_002775.4:c.472+9975G= NP_002766.1:n.472+9975G=
NM_002775.5:c.472+9975G= MANE Select NP_002766.1:n.472+9975G=