Canonical Allele Identifier: CA2142797597

Gene: SPTB

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000389720.4:c.6173C=	ENSP00000374370.4:p.Thr2058=
ENST00000644917.1:c.6173C= MANE Select	ENSP00000495909.1:p.Thr2058=
ENST00000389720.3:c.6173C=	ENSP00000374370.3:p.Thr2058=
ENST00000389721.9:c.6173C=	ENSP00000374371.5:p.Thr2058=
ENST00000389722.7:c.6173C=	ENSP00000374372.3:p.Thr2058=
ENST00000542694.2:n.505C=
ENST00000553938.5:c.2168C=	ENSP00000451324.1:p.Thr723=
ENST00000556626.5:c.6173C=	ENSP00000451752.1:p.Thr2058=
NM_000347.5:c.6173C=	NP_000338.3:p.Thr2058=
NM_001024858.2:c.6173C=	NP_001020029.1:p.Thr2058=
XM_005268023.3:c.6173C=	XP_005268080.1:p.Thr2058=
NM_001024858.3:c.6173C=	NP_001020029.1:p.Thr2058=
NM_001355436.2:c.6173C= MANE Select	NP_001342365.1:p.Thr2058=
NM_001355437.2:c.6173C=	NP_001342366.1:p.Thr2058=
XM_017021612.2:c.6173C=	XP_016877101.1:p.Thr2058=
XM_024449699.1:c.6173C=	XP_024305467.1:p.Thr2058=
NM_001024858.4:c.6173C=	NP_001020029.1:p.Thr2058=