Canonical Allele Identifier: CA1941467408
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472127_122472128delinsTG , CM000672.2:g.122472127_122472128delinsTG GRCh38
NC_000010.10:g.124231643_124231644delinsTG , CM000672.1:g.124231643_124231644delinsTG GRCh37
NC_000010.9:g.124221633_124221634delinsTG NCBI36
NG_011554.1:g.15603_15604delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10003_472+10004delinsTG MANE Select ENSP00000357980.3:n.472+10003_472+10004delinsTG
ENST00000648167.1:c.154+13418_154+13419delinsTG ENSP00000498033.1:n.154+13418_154+13419delinsTG
ENST00000368984.7:c.472+10003_472+10004delinsTG ENSP00000357980.3:n.472+10003_472+10004delinsTG
NM_002775.4:c.472+10003_472+10004delinsTG NP_002766.1:n.472+10003_472+10004delinsTG
NM_002775.5:c.472+10003_472+10004delinsTG MANE Select NP_002766.1:n.472+10003_472+10004delinsTG