Canonical Allele Identifier: CA355975765
Gene: SLBP HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000489418.6:c.453C>A MANE Select ENSP00000417686.1:p.Tyr151Ter
ENST00000318386.8:c.474C>A ENSP00000316490.4:p.Tyr158Ter
ENST00000429429.6:c.336C>A ENSP00000406322.2:p.Tyr112Ter
ENST00000480936.1:c.475C>A
ENST00000483348.5:c.317C>A
ENST00000488267.5:c.348C>A ENSP00000418658.1:p.Tyr116Ter
ENST00000489418.5:c.453C>A ENSP00000417686.1:p.Tyr151Ter
NM_001306074.1:c.348C>A NP_001293003.1:p.Tyr116Ter
NM_001306075.1:c.336C>A NP_001293004.1:p.Tyr112Ter
NM_006527.2:c.453C>A NP_006518.1:p.Tyr151Ter
NM_006527.3:c.453C>A NP_006518.1:p.Tyr151Ter
XR_002959759.1:n.4141C>A
NM_006527.4:c.453C>A MANE Select NP_006518.1:p.Tyr151Ter
NM_001306074.2:c.348C>A NP_001293003.1:p.Tyr116Ter
NM_001306075.2:c.336C>A NP_001293004.1:p.Tyr112Ter