Canonical Allele Identifier: CA1941477309
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506982T= , CM000672.2:g.122506982T= GRCh38
NC_000010.10:g.124266498T= , CM000672.1:g.124266498T= GRCh37
NC_000010.9:g.124256488T= NCBI36
NG_011554.1:g.50458T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+97T= MANE Select ENSP00000357980.3:n.972+97T=
ENST00000648167.1:c.654+97T= ENSP00000498033.1:n.654+97T=
ENST00000368984.7:c.972+97T= ENSP00000357980.3:n.972+97T=
ENST00000420892.1:c.195+97T= ENSP00000412676.1:n.195+97T=
NM_002775.4:c.972+97T= NP_002766.1:n.972+97T=
NM_002775.5:c.972+97T= MANE Select NP_002766.1:n.972+97T=
Search 100 bp 5'
Search 100 bp 3'