Canonical Allele Identifier: CA262681632

Gene: SPTB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64766800G>T , CM000676.2:g.64766800G>T	GRCh38
NC_000014.8:g.65233518G>T , CM000676.1:g.65233518G>T	GRCh37
NC_000014.7:g.64303271G>T	NCBI36
NG_016202.1:g.61349C>A
NG_016202.2:g.118093C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001355436.2:c.6271C>A MANE Select	NP_001342365.1:p.Pro2091Thr
ENST00000644917.1:c.6271C>A MANE Select	ENSP00000495909.1:p.Pro2091Thr
NM_000347.5:c.6271C>A	NP_000338.3:p.Pro2091Thr
NM_001024858.2:c.6271C>A	NP_001020029.1:p.Pro2091Thr
NM_001024858.3:c.6271C>A	NP_001020029.1:p.Pro2091Thr
NM_001024858.4:c.6271C>A	NP_001020029.1:p.Pro2091Thr
NM_001355437.2:c.6271C>A	NP_001342366.1:p.Pro2091Thr
ENST00000389720.3:c.6221C>A	ENSP00000374370.3:p.Ala2074Asp
ENST00000389720.4:c.6271C>A	ENSP00000374370.4:p.Pro2091Thr
ENST00000389721.9:c.6271C>A	ENSP00000374371.5:p.Pro2091Thr
ENST00000389722.7:c.6271C>A	ENSP00000374372.3:p.Pro2091Thr
ENST00000553938.5:c.2266C>A	ENSP00000451324.1:p.Pro756Thr
ENST00000556626.5:c.6271C>A	ENSP00000451752.1:p.Pro2091Thr
XM_005268023.3:c.6271C>A	XP_005268080.1:p.Pro2091Thr
XM_017021612.2:c.6271C>A	XP_016877101.1:p.Pro2091Thr
XM_024449699.1:c.6271C>A	XP_024305467.1:p.Pro2091Thr