Canonical Allele Identifier: CA1619955244

Gene: TAPBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33305078G= , CM000668.2:g.33305078G=	GRCh38
NC_000006.11:g.33272855G= , CM000668.1:g.33272855G=	GRCh37
NC_000006.10:g.33380833G=	NCBI36
NG_009876.1:g.14135C= , LRG_114:g.14135C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003190.5:c.779C= MANE Select	NP_003181.3:p.Thr260=
ENST00000434618.7:c.779C= MANE Select	ENSP00000395701.2:p.Thr260=
NM_003190.4:c.779C= , LRG_114t1:c.779C=	NP_003181.3:p.Thr260=
NM_172208.2:c.779C=	NP_757345.2:p.Thr260=
NM_172208.3:c.779C=	NP_757345.2:p.Thr260=
NM_172209.2:c.518C=	NP_757346.2:p.Thr173=
NM_172209.3:c.518C=	NP_757346.2:p.Thr173=
ENST00000426633.6:c.779C=	ENSP00000404833.2:p.Thr260=
ENST00000434618.6:c.779C=	ENSP00000395701.2:p.Thr260=
ENST00000437116.2:n.779C=
ENST00000456592.3:c.390-697C=	ENSP00000387803.3:n.390-697C=
ENST00000467025.2:c.608C=	ENSP00000417523.2:p.Thr203=
ENST00000475304.5:c.833C=	ENSP00000417949.1:p.Thr278=
ENST00000480730.5:n.787C=
ENST00000489157.5:c.518C=	ENSP00000419659.1:p.Thr173=
ENST00000489157.6:c.518C=	ENSP00000419659.1:p.Thr173=
ENST00000699647.1:n.1238C=
ENST00000699648.1:c.779C=	ENSP00000514499.1:p.Thr260=
ENST00000699649.1:c.227C=	ENSP00000514500.1:p.Thr76=
ENST00000699650.1:c.503C=	ENSP00000514501.1:p.Thr168=
ENST00000699651.1:c.227C=	ENSP00000514502.1:p.Thr76=
ENST00000699652.1:c.779C=	ENSP00000514503.1:p.Thr260=
ENST00000699653.1:n.1167C=
ENST00000699654.1:c.518C=	ENSP00000514504.1:p.Thr173=
ENST00000699655.1:n.992C=
ENST00000699656.1:c.779C=	ENSP00000514505.1:p.Thr260=
ENST00000699657.1:c.779C=	ENSP00000514506.1:p.Thr260=
ENST00000699659.1:c.779C=	ENSP00000514507.1:p.Thr260=
ENST00000699660.1:n.992C=
ENST00000699661.1:n.992C=
ENST00000699662.1:n.623C=
ENST00000699663.1:n.992C=
ENST00000699664.1:n.992C=
XM_011514828.1:c.779C=	XP_011513130.1:p.Thr260=
XM_011514828.3:c.779C=	XP_011513130.1:p.Thr260=
XM_017011227.1:c.779C=	XP_016866716.1:p.Thr260=