Canonical Allele Identifier: CA390039257
Gene: SPTB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64767709G>T , CM000676.2:g.64767709G>T GRCh38
NC_000014.8:g.65234427G>T , CM000676.1:g.65234427G>T GRCh37
NC_000014.7:g.64304180G>T NCBI36
NG_016202.1:g.60440C>A
NG_016202.2:g.117184C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389720.4:c.6173C>A ENSP00000374370.4:p.Thr2058Lys
ENST00000644917.1:c.6173C>A MANE Select ENSP00000495909.1:p.Thr2058Lys
ENST00000389720.3:c.6173C>A ENSP00000374370.3:p.Thr2058Lys
ENST00000389721.9:c.6173C>A ENSP00000374371.5:p.Thr2058Lys
ENST00000389722.7:c.6173C>A ENSP00000374372.3:p.Thr2058Lys
ENST00000542694.2:n.505C>A
ENST00000553938.5:c.2168C>A ENSP00000451324.1:p.Thr723Lys
ENST00000556626.5:c.6173C>A ENSP00000451752.1:p.Thr2058Lys
NM_000347.5:c.6173C>A NP_000338.3:p.Thr2058Lys
NM_001024858.2:c.6173C>A NP_001020029.1:p.Thr2058Lys
XM_005268023.3:c.6173C>A XP_005268080.1:p.Thr2058Lys
NM_001024858.3:c.6173C>A NP_001020029.1:p.Thr2058Lys
NM_001355436.2:c.6173C>A MANE Select NP_001342365.1:p.Thr2058Lys
NM_001355437.2:c.6173C>A NP_001342366.1:p.Thr2058Lys
XM_017021612.2:c.6173C>A XP_016877101.1:p.Thr2058Lys
XM_024449699.1:c.6173C>A XP_024305467.1:p.Thr2058Lys
NM_001024858.4:c.6173C>A NP_001020029.1:p.Thr2058Lys