Canonical Allele Identifier: CA995498201
Gene: TYROBP HGNC NCBI

Linked Data

dbSNP Id: rs1396887951

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35907636dup , CM000681.2:g.35907636dup GRCh38
NC_000019.9:g.36398538dup , CM000681.1:g.36398538dup GRCh37
NC_000019.8:g.41090378dup NCBI36
NG_009304.1:g.5654dup , LRG_607:g.5654dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262629.9:c.95-51dup MANE Select ENSP00000262629.3:n.95-51dup
ENST00000262629.8:c.95-51dup ENSP00000262629.3:n.95-51dup
ENST00000424586.7:c.62-51dup ENSP00000402371.3:n.62-51dup
ENST00000544690.6:c.62-51dup ENSP00000445332.1:n.62-51dup
ENST00000585626.1:n.162-51dup
ENST00000585901.6:c.95-51dup ENSP00000468608.1:n.95-51dup
ENST00000586946.1:c.88-51dup ENSP00000465656.1:n.88-51dup
ENST00000587837.5:c.88-51dup ENSP00000465081.1:n.88-51dup
ENST00000588439.1:n.188dup
ENST00000589517.1:c.95-51dup ENSP00000468447.1:n.95-51dup
NM_001173514.1:c.62-51dup NP_001166985.1:n.62-51dup
NM_001173515.1:c.62-51dup NP_001166986.1:n.62-51dup
NM_003332.3:c.95-51dup , LRG_607t1:c.95-51dup NP_003323.1:n.95-51dup
NM_198125.2:c.95-51dup NP_937758.1:n.95-51dup
NR_033390.1:n.136-51dup
NM_001173514.2:c.62-51dup NP_001166985.1:n.62-51dup
NM_001173515.2:c.62-51dup NP_001166986.1:n.62-51dup
NM_003332.4:c.95-51dup MANE Select NP_003323.1:n.95-51dup
NM_198125.3:c.95-51dup NP_937758.1:n.95-51dup
NR_033390.2:n.122-51dup