Canonical Allele Identifier: CA1876129290

Gene: BRINP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.119339356C= , CM000671.2:g.119339356C=	GRCh38
NC_000009.11:g.122101634C= , CM000671.1:g.122101634C=	GRCh37
NC_000009.10:g.121141455C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265922.8:c.-50-25951G= MANE Select	ENSP00000265922.2:n.-50-25951G=
ENST00000265922.7:c.-50-25951G=	ENSP00000265922.2:n.-50-25951G=
ENST00000373964.2:c.-50-25951G=	ENSP00000363075.1:n.-50-25951G=
NM_014618.2:c.-50-25951G=	NP_055433.2:n.-50-25951G=
NM_014618.3:c.-50-25951G= MANE Select	NP_055433.2:n.-50-25951G=