Canonical Allele Identifier: CA1941477408
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507179_122507180delinsAC , CM000672.2:g.122507179_122507180delinsAC GRCh38
NC_000010.10:g.124266695_124266696delinsAC , CM000672.1:g.124266695_124266696delinsAC GRCh37
NC_000010.9:g.124256685_124256686delinsAC NCBI36
NG_011554.1:g.50655_50656delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-191_973-190delinsAC MANE Select ENSP00000357980.3:n.973-191_973-190delinsAC
ENST00000648167.1:c.655-191_655-190delinsAC ENSP00000498033.1:n.655-191_655-190delinsAC
ENST00000368984.7:c.973-191_973-190delinsAC ENSP00000357980.3:n.973-191_973-190delinsAC
ENST00000420892.1:c.196-191_196-190delinsAC ENSP00000412676.1:n.196-191_196-190delinsAC
NM_002775.4:c.973-191_973-190delinsAC NP_002766.1:n.973-191_973-190delinsAC
NM_002775.5:c.973-191_973-190delinsAC MANE Select NP_002766.1:n.973-191_973-190delinsAC