Canonical Allele Identifier: CA2529623454

Gene: SPTB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64767440_64767457dup , CM000676.2:g.64767440_64767457dup	GRCh38
NC_000014.8:g.65234158_65234175dup , CM000676.1:g.65234158_65234175dup	GRCh37
NC_000014.7:g.64303911_64303928dup	NCBI36
NG_016202.1:g.60695_60712dup
NG_016202.2:g.117439_117456dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389720.4:c.6220-102_6220-85dup	ENSP00000374370.4:n.6220-102_6220-85dup
ENST00000644917.1:c.6220-102_6220-85dup MANE Select	ENSP00000495909.1:n.6220-102_6220-85dup
ENST00000389720.3:c.6219+209_6219+226dup	ENSP00000374370.3:n.6219+209_6219+226dup
ENST00000389721.9:c.6220-102_6220-85dup	ENSP00000374371.5:n.6220-102_6220-85dup
ENST00000389722.7:c.6220-102_6220-85dup	ENSP00000374372.3:n.6220-102_6220-85dup
ENST00000542694.2:n.552-102_552-85dup
ENST00000553938.5:c.2215-102_2215-85dup	ENSP00000451324.1:n.2215-102_2215-85dup
ENST00000556626.5:c.6220-102_6220-85dup	ENSP00000451752.1:n.6220-102_6220-85dup
NM_000347.5:c.6220-102_6220-85dup	NP_000338.3:n.6220-102_6220-85dup
NM_001024858.2:c.6220-102_6220-85dup	NP_001020029.1:n.6220-102_6220-85dup
XM_005268023.3:c.6220-102_6220-85dup	XP_005268080.1:n.6220-102_6220-85dup
NM_001024858.3:c.6220-102_6220-85dup	NP_001020029.1:n.6220-102_6220-85dup
NM_001355436.2:c.6220-102_6220-85dup MANE Select	NP_001342365.1:n.6220-102_6220-85dup
NM_001355437.2:c.6220-102_6220-85dup	NP_001342366.1:n.6220-102_6220-85dup
XM_017021612.2:c.6220-102_6220-85dup	XP_016877101.1:n.6220-102_6220-85dup
XM_024449699.1:c.6220-102_6220-85dup	XP_024305467.1:n.6220-102_6220-85dup
NM_001024858.4:c.6220-102_6220-85dup	NP_001020029.1:n.6220-102_6220-85dup