Canonical Allele Identifier: CA12999519
Gene: BRINP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.119297431T>C , CM000671.2:g.119297431T>C GRCh38
NC_000009.11:g.122059709T>C , CM000671.1:g.122059709T>C GRCh37
NC_000009.10:g.121099530T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265922.8:c.218+15707A>G MANE Select ENSP00000265922.2:n.218+15707A>G
ENST00000265922.7:c.218+15707A>G ENSP00000265922.2:n.218+15707A>G
ENST00000373964.2:c.218+15707A>G ENSP00000363075.1:n.218+15707A>G
NM_014618.2:c.218+15707A>G NP_055433.2:n.218+15707A>G
NM_014618.3:c.218+15707A>G MANE Select NP_055433.2:n.218+15707A>G