Canonical Allele Identifier: CA1128670080

Gene: BRINP1

Linked Data

• dbSNP Id: rs1830047046
• gnomAD v3: 9-119222132-CT-C
• gnomAD v4: 9-119222132-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.119222137del , CM000671.2:g.119222137del	GRCh38
NC_000009.11:g.121984415del , CM000671.1:g.121984415del	GRCh37
NC_000009.10:g.121024236del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265922.8:c.686-7978del MANE Select	ENSP00000265922.2:n.686-7978del
ENST00000265922.7:c.686-7978del	ENSP00000265922.2:n.686-7978del
ENST00000373964.2:c.686-7978del	ENSP00000363075.1:n.686-7978del
NM_014618.2:c.686-7978del	NP_055433.2:n.686-7978del
NM_014618.3:c.686-7978del MANE Select	NP_055433.2:n.686-7978del