Canonical Allele Identifier: CA889322218

Gene: SELENBP1

Linked Data

• dbSNP Id: rs1205821737
• MyVariant Identifiers: chr1:g.151344676A>C (hg19) ; chr1:g.151372200A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151372200A>C , CM000663.2:g.151372200A>C	GRCh38
NC_000001.10:g.151344676A>C , CM000663.1:g.151344676A>C	GRCh37
NC_000001.9:g.149611300A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368868.10:c.4+438T>G MANE Select	ENSP00000357861.5:n.4+438T>G
ENST00000368868.9:c.4+438T>G	ENSP00000357861.5:n.4+438T>G
ENST00000423070.5:c.-80+438T>G	ENSP00000416206.1:n.-80+438T>G
ENST00000426705.6:c.-80+438T>G	ENSP00000397261.2:n.-80+438T>G
ENST00000427977.6:c.4+438T>G	ENSP00000412816.1:n.4+438T>G
ENST00000443708.5:c.4+438T>G	ENSP00000402531.1:n.4+438T>G
ENST00000447402.7:c.4+438T>G	ENSP00000413960.3:n.4+438T>G
ENST00000455397.5:c.4+438T>G	ENSP00000395637.1:n.4+438T>G
ENST00000455839.5:c.4+438T>G	ENSP00000390433.1:n.4+438T>G
ENST00000458566.5:c.4+438T>G	ENSP00000406222.1:n.4+438T>G
ENST00000463664.5:n.57+438T>G
ENST00000470345.5:n.69+438T>G
ENST00000473693.5:n.68+438T>G
ENST00000474352.5:n.68+438T>G
ENST00000492643.5:n.70+438T>G
ENST00000493560.5:n.57+438T>G
ENST00000498494.1:n.54+438T>G
NM_001258288.1:c.4+438T>G	NP_001245217.1:n.4+438T>G
NM_001258289.1:c.-80+438T>G	NP_001245218.1:n.-80+438T>G
NM_003944.3:c.4+438T>G	NP_003935.2:n.4+438T>G
XM_011510110.1:c.-35+438T>G	XP_011508412.1:n.-35+438T>G
XR_921993.1:n.84+438T>G
XM_024450671.1:c.-1161+438T>G	XP_024306439.1:n.-1161+438T>G
XR_002957987.1:n.88+438T>G
XR_921993.2:n.76+438T>G
NM_003944.4:c.4+438T>G MANE Select	NP_003935.2:n.4+438T>G
NM_001258288.2:c.4+438T>G	NP_001245217.1:n.4+438T>G
NM_001258289.2:c.-80+438T>G	NP_001245218.1:n.-80+438T>G