Canonical Allele Identifier: CA1941477242
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506822C= , CM000672.2:g.122506822C= GRCh38
NC_000010.10:g.124266338C= , CM000672.1:g.124266338C= GRCh37
NC_000010.9:g.124256328C= NCBI36
NG_011554.1:g.50298C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.909C= MANE Select ENSP00000357980.3:p.Gly303=
ENST00000648167.1:c.591C= ENSP00000498033.1:p.Gly197=
ENST00000368984.7:c.909C= ENSP00000357980.3:p.Gly303=
ENST00000420892.1:c.132C= ENSP00000412676.1:p.Gly44=
NM_002775.4:c.909C= NP_002766.1:p.Gly303=
NM_002775.5:c.909C= MANE Select NP_002766.1:p.Gly303=