Canonical Allele Identifier: CA1433431040
Gene: SLBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1699590G= , CM000666.2:g.1699590G= GRCh38
NC_000004.11:g.1701317G= , CM000666.1:g.1701317G= GRCh37
NC_000004.10:g.1671115G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000489418.6:c.453C= MANE Select ENSP00000417686.1:p.Tyr151=
ENST00000318386.8:c.474C= ENSP00000316490.4:p.Tyr158=
ENST00000429429.6:c.336C= ENSP00000406322.2:p.Tyr112=
ENST00000480936.1:c.475C=
ENST00000483348.5:c.317C=
ENST00000488267.5:c.348C= ENSP00000418658.1:p.Tyr116=
ENST00000489418.5:c.453C= ENSP00000417686.1:p.Tyr151=
NM_001306074.1:c.348C= NP_001293003.1:p.Tyr116=
NM_001306075.1:c.336C= NP_001293004.1:p.Tyr112=
NM_006527.2:c.453C= NP_006518.1:p.Tyr151=
NM_006527.3:c.453C= NP_006518.1:p.Tyr151=
XR_002959759.1:n.4141C=
NM_006527.4:c.453C= MANE Select NP_006518.1:p.Tyr151=
NM_001306074.2:c.348C= NP_001293003.1:p.Tyr116=
NM_001306075.2:c.336C= NP_001293004.1:p.Tyr112=