Canonical Allele Identifier: CA2584619743
Gene: TYROBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35908129C>G , CM000681.2:g.35908129C>G GRCh38
NC_000019.9:g.36399031C>G , CM000681.1:g.36399031C>G GRCh37
NC_000019.8:g.41090871C>G NCBI36
NG_009304.1:g.5156G>C , LRG_607:g.5156G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262629.9:c.61+39G>C MANE Select ENSP00000262629.3:n.61+39G>C
ENST00000262629.8:c.61+39G>C ENSP00000262629.3:n.61+39G>C
ENST00000424586.7:c.61+39G>C ENSP00000402371.3:n.61+39G>C
ENST00000544690.6:c.61+39G>C ENSP00000445332.1:n.61+39G>C
ENST00000585626.1:n.128+39G>C
ENST00000585901.6:c.61+39G>C ENSP00000468608.1:n.61+39G>C
ENST00000586946.1:c.54+46G>C ENSP00000465656.1:n.54+46G>C
ENST00000587837.5:c.54+46G>C ENSP00000465081.1:n.54+46G>C
ENST00000588439.1:n.56+39G>C
ENST00000589517.1:c.61+39G>C ENSP00000468447.1:n.61+39G>C
NM_001173514.1:c.61+39G>C NP_001166985.1:n.61+39G>C
NM_001173515.1:c.61+39G>C NP_001166986.1:n.61+39G>C
NM_003332.3:c.61+39G>C , LRG_607t1:c.61+39G>C NP_003323.1:n.61+39G>C
NM_198125.2:c.61+39G>C NP_937758.1:n.61+39G>C
NR_033390.1:n.135+46G>C
NM_001173514.2:c.61+39G>C NP_001166985.1:n.61+39G>C
NM_001173515.2:c.61+39G>C NP_001166986.1:n.61+39G>C
NM_003332.4:c.61+39G>C MANE Select NP_003323.1:n.61+39G>C
NM_198125.3:c.61+39G>C NP_937758.1:n.61+39G>C
NR_033390.2:n.121+46G>C