Canonical Allele Identifier: CA1876072930

Gene: BRINP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.119222145C= , CM000671.2:g.119222145C=	GRCh38
NC_000009.11:g.121984423C= , CM000671.1:g.121984423C=	GRCh37
NC_000009.10:g.121024244C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265922.8:c.686-7990G= MANE Select	ENSP00000265922.2:n.686-7990G=
ENST00000265922.7:c.686-7990G=	ENSP00000265922.2:n.686-7990G=
ENST00000373964.2:c.686-7990G=	ENSP00000363075.1:n.686-7990G=
NM_014618.2:c.686-7990G=	NP_055433.2:n.686-7990G=
NM_014618.3:c.686-7990G= MANE Select	NP_055433.2:n.686-7990G=