Canonical Allele Identifier: CA1128670204
Gene: BRINP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.119222365G>A , CM000671.2:g.119222365G>A GRCh38
NC_000009.11:g.121984643G>A , CM000671.1:g.121984643G>A GRCh37
NC_000009.10:g.121024464G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265922.8:c.686-8210C>T MANE Select ENSP00000265922.2:n.686-8210C>T
ENST00000265922.7:c.686-8210C>T ENSP00000265922.2:n.686-8210C>T
ENST00000373964.2:c.686-8210C>T ENSP00000363075.1:n.686-8210C>T
NM_014618.2:c.686-8210C>T NP_055433.2:n.686-8210C>T
NM_014618.3:c.686-8210C>T MANE Select NP_055433.2:n.686-8210C>T