Canonical Allele Identifier: CA1941472737
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122496794T= , CM000672.2:g.122496794T= GRCh38
NC_000010.10:g.124256310T= , CM000672.1:g.124256310T= GRCh37
NC_000010.9:g.124246300T= NCBI36
NG_011554.1:g.40270T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.777+7168T= MANE Select ENSP00000357980.3:n.777+7168T=
ENST00000648167.1:c.459+7168T= ENSP00000498033.1:n.459+7168T=
ENST00000368984.7:c.777+7168T= ENSP00000357980.3:n.777+7168T=
NM_002775.4:c.777+7168T= NP_002766.1:n.777+7168T=
NM_002775.5:c.777+7168T= MANE Select NP_002766.1:n.777+7168T=
Search 100 bp 5'
Search 100 bp 3'