Canonical Allele Identifier: CA1941478120
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508745G= , CM000672.2:g.122508745G= GRCh38
NC_000010.10:g.124268261G= , CM000672.1:g.124268261G= GRCh37
NC_000010.9:g.124258251G= NCBI36
NG_011554.1:g.52221G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1095G= MANE Select ENSP00000357980.3:p.Thr365=
ENST00000648167.1:c.777G= ENSP00000498033.1:p.Thr259=
ENST00000368984.7:c.1095G= ENSP00000357980.3:p.Thr365=
ENST00000420892.1:c.318G= ENSP00000412676.1:p.Thr106=
NM_002775.4:c.1095G= NP_002766.1:p.Thr365=
NM_002775.5:c.1095G= MANE Select NP_002766.1:p.Thr365=
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