Canonical Allele Identifier: CA7231325

Gene: SPTB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64800858C>T , CM000676.2:g.64800858C>T	GRCh38
NC_000014.8:g.65267576C>T , CM000676.1:g.65267576C>T	GRCh37
NC_000014.7:g.64337329C>T	NCBI36
NG_016202.1:g.27291G>A
NG_016202.2:g.84035G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001355436.2:c.774G>A MANE Select	NP_001342365.1:p.Thr258=
ENST00000644917.1:c.774G>A MANE Select	ENSP00000495909.1:p.Thr258=
NM_000347.5:c.774G>A	NP_000338.3:p.Thr258=
NM_001024858.2:c.774G>A	NP_001020029.1:p.Thr258=
NM_001024858.3:c.774G>A	NP_001020029.1:p.Thr258=
NM_001024858.4:c.774G>A	NP_001020029.1:p.Thr258=
NM_001355437.2:c.774G>A	NP_001342366.1:p.Thr258=
ENST00000389720.3:c.774G>A	ENSP00000374370.3:p.Thr258=
ENST00000389720.4:c.774G>A	ENSP00000374370.4:p.Thr258=
ENST00000389721.9:c.774G>A	ENSP00000374371.5:p.Thr258=
ENST00000389722.7:c.774G>A	ENSP00000374372.3:p.Thr258=
ENST00000556626.5:c.774G>A	ENSP00000451752.1:p.Thr258=
XM_005268023.3:c.774G>A	XP_005268080.1:p.Thr258=
XM_011537105.1:c.774G>A	XP_011535407.1:p.Thr258=
XM_011537105.3:c.774G>A	XP_011535407.1:p.Thr258=
XM_017021612.2:c.774G>A	XP_016877101.1:p.Thr258=
XM_024449699.1:c.774G>A	XP_024305467.1:p.Thr258=