Canonical Allele Identifier: CA405388483

Gene: TYROBP

Linked Data

• MyVariant Identifiers: chr19:g.36398479C>A (hg19) ; chr19:g.35907577C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907577C>A , CM000681.2:g.35907577C>A	GRCh38
NC_000019.9:g.36398479C>A , CM000681.1:g.36398479C>A	GRCh37
NC_000019.8:g.41090319C>A	NCBI36
NG_009304.1:g.5708G>T , LRG_607:g.5708G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.98G>T MANE Select	ENSP00000262629.3:p.Cys33Phe
ENST00000262629.8:c.98G>T	ENSP00000262629.3:p.Cys33Phe
ENST00000424586.7:c.65G>T	ENSP00000402371.3:p.Cys22Phe
ENST00000544690.6:c.65G>T	ENSP00000445332.1:p.Cys22Phe
ENST00000585626.1:n.165G>T
ENST00000585901.6:c.98G>T	ENSP00000468608.1:p.Cys33Phe
ENST00000586946.1:c.91G>T	ENSP00000465656.1:p.Ala31Ser
ENST00000587837.5:c.91G>T	ENSP00000465081.1:p.Ala31Ser
ENST00000588439.1:n.242G>T
ENST00000589517.1:c.98G>T	ENSP00000468447.1:p.Cys33Phe
NM_001173514.1:c.65G>T	NP_001166985.1:p.Cys22Phe
NM_001173515.1:c.65G>T	NP_001166986.1:p.Cys22Phe
NM_003332.3:c.98G>T , LRG_607t1:c.98G>T	NP_003323.1:p.Cys33Phe
NM_198125.2:c.98G>T	NP_937758.1:p.Cys33Phe
NR_033390.1:n.139G>T
NM_001173514.2:c.65G>T	NP_001166985.1:p.Cys22Phe
NM_001173515.2:c.65G>T	NP_001166986.1:p.Cys22Phe
NM_003332.4:c.98G>T MANE Select	NP_003323.1:p.Cys33Phe
NM_198125.3:c.98G>T	NP_937758.1:p.Cys33Phe
NR_033390.2:n.125G>T