Canonical Allele Identifier: CA2479556783

Gene: SELENBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151372470G= , CM000663.2:g.151372470G=	GRCh38
NC_000001.10:g.151344946G= , CM000663.1:g.151344946G=	GRCh37
NC_000001.9:g.149611570G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368868.10:c.4+168C= MANE Select	ENSP00000357861.5:n.4+168C=
ENST00000368868.9:c.4+168C=	ENSP00000357861.5:n.4+168C=
ENST00000423070.5:c.-80+168C=	ENSP00000416206.1:n.-80+168C=
ENST00000426705.6:c.-80+168C=	ENSP00000397261.2:n.-80+168C=
ENST00000427977.6:c.4+168C=	ENSP00000412816.1:n.4+168C=
ENST00000443708.5:c.4+168C=	ENSP00000402531.1:n.4+168C=
ENST00000447402.7:c.4+168C=	ENSP00000413960.3:n.4+168C=
ENST00000455397.5:c.4+168C=	ENSP00000395637.1:n.4+168C=
ENST00000455839.5:c.4+168C=	ENSP00000390433.1:n.4+168C=
ENST00000458566.5:c.4+168C=	ENSP00000406222.1:n.4+168C=
ENST00000463664.5:n.57+168C=
ENST00000470345.5:n.69+168C=
ENST00000473693.5:n.68+168C=
ENST00000474352.5:n.68+168C=
ENST00000492643.5:n.70+168C=
ENST00000493560.5:n.57+168C=
ENST00000498494.1:n.54+168C=
NM_001258288.1:c.4+168C=	NP_001245217.1:n.4+168C=
NM_001258289.1:c.-80+168C=	NP_001245218.1:n.-80+168C=
NM_003944.3:c.4+168C=	NP_003935.2:n.4+168C=
XM_011510110.1:c.-35+168C=	XP_011508412.1:n.-35+168C=
XR_921993.1:n.84+168C=
XM_024450671.1:c.-1161+168C=	XP_024306439.1:n.-1161+168C=
XR_002957987.1:n.88+168C=
XR_921993.2:n.76+168C=
NM_003944.4:c.4+168C= MANE Select	NP_003935.2:n.4+168C=
NM_001258288.2:c.4+168C=	NP_001245217.1:n.4+168C=
NM_001258289.2:c.-80+168C=	NP_001245218.1:n.-80+168C=