Canonical Allele Identifier: CA1941459111
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461582T= , CM000672.2:g.122461582T= GRCh38
NC_000010.10:g.124221098T= , CM000672.1:g.124221098T= GRCh37
NC_000010.9:g.124211088T= NCBI36
NG_011554.1:g.5058T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-71T= MANE Select ENSP00000357980.3:n.-71T=
ENST00000648167.1:c.154+2873T= ENSP00000498033.1:n.154+2873T=
ENST00000368984.7:c.-71T= ENSP00000357980.3:n.-71T=
NM_002775.4:c.-71T= NP_002766.1:n.-71T=
NM_002775.5:c.-71T= MANE Select NP_002766.1:n.-71T=