Canonical Allele Identifier: CA1941467333
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122471962A= , CM000672.2:g.122471962A= GRCh38
NC_000010.10:g.124231478A= , CM000672.1:g.124231478A= GRCh37
NC_000010.9:g.124221468A= NCBI36
NG_011554.1:g.15438A=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.472+9838A= MANE Select ENSP00000357980.3:n.472+9838A=
ENST00000648167.1:c.154+13253A= ENSP00000498033.1:n.154+13253A=
ENST00000368984.7:c.472+9838A= ENSP00000357980.3:n.472+9838A=
NM_002775.4:c.472+9838A= NP_002766.1:n.472+9838A=
NM_002775.5:c.472+9838A= MANE Select NP_002766.1:n.472+9838A=