Canonical Allele Identifier: CA1876129310
Gene: BRINP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.119339394A= , CM000671.2:g.119339394A= GRCh38
NC_000009.11:g.122101672A= , CM000671.1:g.122101672A= GRCh37
NC_000009.10:g.121141493A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265922.8:c.-50-25989T= MANE Select ENSP00000265922.2:n.-50-25989T=
ENST00000265922.7:c.-50-25989T= ENSP00000265922.2:n.-50-25989T=
ENST00000373964.2:c.-50-25989T= ENSP00000363075.1:n.-50-25989T=
NM_014618.2:c.-50-25989T= NP_055433.2:n.-50-25989T=
NM_014618.3:c.-50-25989T= MANE Select NP_055433.2:n.-50-25989T=
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