Canonical Allele Identifier: CA1876073084
Gene: BRINP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.119222312A= , CM000671.2:g.119222312A= GRCh38
NC_000009.11:g.121984590A= , CM000671.1:g.121984590A= GRCh37
NC_000009.10:g.121024411A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265922.8:c.686-8157T= MANE Select ENSP00000265922.2:n.686-8157T=
ENST00000265922.7:c.686-8157T= ENSP00000265922.2:n.686-8157T=
ENST00000373964.2:c.686-8157T= ENSP00000363075.1:n.686-8157T=
NM_014618.2:c.686-8157T= NP_055433.2:n.686-8157T=
NM_014618.3:c.686-8157T= MANE Select NP_055433.2:n.686-8157T=
Search 100 bp 5'
Search 100 bp 3'