Canonical Allele Identifier: CA1941478113
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508736G= , CM000672.2:g.122508736G= GRCh38
NC_000010.10:g.124268252G= , CM000672.1:g.124268252G= GRCh37
NC_000010.9:g.124258242G= NCBI36
NG_011554.1:g.52212G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1086G= MANE Select ENSP00000357980.3:p.Lys362=
ENST00000648167.1:c.768G= ENSP00000498033.1:p.Lys256=
ENST00000368984.7:c.1086G= ENSP00000357980.3:p.Lys362=
ENST00000420892.1:c.309G= ENSP00000412676.1:p.Lys103=
NM_002775.4:c.1086G= NP_002766.1:p.Lys362=
NM_002775.5:c.1086G= MANE Select NP_002766.1:p.Lys362=