Canonical Allele Identifier: CA1941472783
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122496930T= , CM000672.2:g.122496930T= GRCh38
NC_000010.10:g.124256446T= , CM000672.1:g.124256446T= GRCh37
NC_000010.9:g.124246436T= NCBI36
NG_011554.1:g.40406T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.777+7304T= MANE Select ENSP00000357980.3:n.777+7304T=
ENST00000648167.1:c.459+7304T= ENSP00000498033.1:n.459+7304T=
ENST00000368984.7:c.777+7304T= ENSP00000357980.3:n.777+7304T=
NM_002775.4:c.777+7304T= NP_002766.1:n.777+7304T=
NM_002775.5:c.777+7304T= MANE Select NP_002766.1:n.777+7304T=