Canonical Allele Identifier: CA2142804034

Gene: SPTB

Linked Data

• dbSNP Id: rs2082297522

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64772768del , CM000676.2:g.64772768del	GRCh38
NC_000014.8:g.65239486del , CM000676.1:g.65239486del	GRCh37
NC_000014.7:g.64309239del	NCBI36
NG_016202.1:g.55381del
NG_016202.2:g.112125del

Transcript Alleles

HGVS	Amino-acid change
ENST00000389720.4:c.5365del	ENSP00000374370.4:p.Arg1789AlafsTer?
ENST00000644917.1:c.5365del MANE Select	ENSP00000495909.1:p.Arg1789AlafsTer?
ENST00000389720.3:c.5365del	ENSP00000374370.3:p.Arg1789AlafsTer?
ENST00000389721.9:c.5365del	ENSP00000374371.5:p.Arg1789AlafsTer?
ENST00000389722.7:c.5365del	ENSP00000374372.3:p.Arg1789AlafsTer?
ENST00000553938.5:c.1360del	ENSP00000451324.1:p.Arg454AlafsTer?
ENST00000556626.5:c.5365del	ENSP00000451752.1:p.Arg1789AlafsTer?
NM_000347.5:c.5365del	NP_000338.3:p.Arg1789AlafsTer?
NM_001024858.2:c.5365del	NP_001020029.1:p.Arg1789AlafsTer?
XM_005268023.3:c.5365del	XP_005268080.1:p.Arg1789AlafsTer?
NM_001024858.3:c.5365del	NP_001020029.1:p.Arg1789AlafsTer?
NM_001355436.2:c.5365del MANE Select	NP_001342365.1:p.Arg1789AlafsTer?
NM_001355437.2:c.5365del	NP_001342366.1:p.Arg1789AlafsTer?
XM_017021612.2:c.5365del	XP_016877101.1:p.Arg1789AlafsTer?
XM_024449699.1:c.5365del	XP_024305467.1:p.Arg1789AlafsTer?
NM_001024858.4:c.5365del	NP_001020029.1:p.Arg1789AlafsTer?