Canonical Allele Identifier: CA2142804295
Gene: SPTB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64772870C= , CM000676.2:g.64772870C= GRCh38
NC_000014.8:g.65239588C= , CM000676.1:g.65239588C= GRCh37
NC_000014.7:g.64309341C= NCBI36
NG_016202.1:g.55279G=
NG_016202.2:g.112023G=

Transcript Alleles

HGVS Amino-acid change
ENST00000389720.4:c.5263G= ENSP00000374370.4:p.Glu1755=
ENST00000644917.1:c.5263G= MANE Select ENSP00000495909.1:p.Glu1755=
ENST00000389720.3:c.5263G= ENSP00000374370.3:p.Glu1755=
ENST00000389721.9:c.5263G= ENSP00000374371.5:p.Glu1755=
ENST00000389722.7:c.5263G= ENSP00000374372.3:p.Glu1755=
ENST00000553938.5:c.1258G= ENSP00000451324.1:p.Glu420=
ENST00000556626.5:c.5263G= ENSP00000451752.1:p.Glu1755=
NM_000347.5:c.5263G= NP_000338.3:p.Glu1755=
NM_001024858.2:c.5263G= NP_001020029.1:p.Glu1755=
XM_005268023.3:c.5263G= XP_005268080.1:p.Glu1755=
NM_001024858.3:c.5263G= NP_001020029.1:p.Glu1755=
NM_001355436.2:c.5263G= MANE Select NP_001342365.1:p.Glu1755=
NM_001355437.2:c.5263G= NP_001342366.1:p.Glu1755=
XM_017021612.2:c.5263G= XP_016877101.1:p.Glu1755=
XM_024449699.1:c.5263G= XP_024305467.1:p.Glu1755=
NM_001024858.4:c.5263G= NP_001020029.1:p.Glu1755=