Canonical Allele Identifier: CA2695213170
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461813_122461814insAG , CM000672.2:g.122461813_122461814insAG GRCh38
NC_000010.10:g.124221329_124221330insAG , CM000672.1:g.124221329_124221330insAG GRCh37
NC_000010.9:g.124211319_124211320insAG NCBI36
NG_011554.1:g.5289_5290insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.161_162insAG MANE Select ENSP00000357980.3:p.Gly56AlafsTer?
ENST00000648167.1:c.154+3104_154+3105insAG ENSP00000498033.1:n.154+3104_154+3105insAG
ENST00000368984.7:c.161_162insAG ENSP00000357980.3:p.Gly56AlafsTer?
NM_002775.4:c.161_162insAG NP_002766.1:p.Gly56AlafsTer?
NM_002775.5:c.161_162insAG MANE Select NP_002766.1:p.Gly56AlafsTer?