Canonical Allele Identifier: CA1941467536
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472362_122472374delinsTTTATTACTATTA , CM000672.2:g.122472362_122472374delinsTTTATTACTATTA GRCh38
NC_000010.10:g.124231878_124231890delinsTTTATTACTATTA , CM000672.1:g.124231878_124231890delinsTTTATTACTATTA GRCh37
NC_000010.9:g.124221868_124221880delinsTTTATTACTATTA NCBI36
NG_011554.1:g.15838_15850delinsTTTATTACTATTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10238_472+10250delinsTTTATTACTATTA MANE Select ENSP00000357980.3:n.472+10238_472+10250delinsTTTATTACTATTA
ENST00000648167.1:c.154+13653_154+13665delinsTTTATTACTATTA ENSP00000498033.1:n.154+13653_154+13665delinsTTTATTACTATTA
ENST00000368984.7:c.472+10238_472+10250delinsTTTATTACTATTA ENSP00000357980.3:n.472+10238_472+10250delinsTTTATTACTATTA
NM_002775.4:c.472+10238_472+10250delinsTTTATTACTATTA NP_002766.1:n.472+10238_472+10250delinsTTTATTACTATTA
NM_002775.5:c.472+10238_472+10250delinsTTTATTACTATTA MANE Select NP_002766.1:n.472+10238_472+10250delinsTTTATTACTATTA