Canonical Allele Identifier: CA405388149

Gene: TYROBP

Linked Data

• MyVariant Identifiers: chr19:g.36398428T>A (hg19) ; chr19:g.35907526T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907526T>A , CM000681.2:g.35907526T>A	GRCh38
NC_000019.9:g.36398428T>A , CM000681.1:g.36398428T>A	GRCh37
NC_000019.8:g.41090268T>A	NCBI36
NG_009304.1:g.5759A>T , LRG_607:g.5759A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.149A>T MANE Select	ENSP00000262629.3:p.Asp50Val
ENST00000262629.8:c.149A>T	ENSP00000262629.3:p.Asp50Val
ENST00000424586.7:c.116A>T	ENSP00000402371.3:p.Asp39Val
ENST00000544690.6:c.116A>T	ENSP00000445332.1:p.Asp39Val
ENST00000585626.1:n.216A>T
ENST00000585901.6:c.149A>T	ENSP00000468608.1:p.Asp50Val
ENST00000586946.1:c.*34A>T	ENSP00000465656.1:n.*34A>T
ENST00000587837.5:c.*34A>T	ENSP00000465081.1:n.*34A>T
ENST00000588439.1:n.293A>T
ENST00000589517.1:c.149A>T	ENSP00000468447.1:p.Asp50Val
NM_001173514.1:c.116A>T	NP_001166985.1:p.Asp39Val
NM_001173515.1:c.116A>T	NP_001166986.1:p.Asp39Val
NM_003332.3:c.149A>T , LRG_607t1:c.149A>T	NP_003323.1:p.Asp50Val
NM_198125.2:c.149A>T	NP_937758.1:p.Asp50Val
NR_033390.1:n.190A>T
NM_001173514.2:c.116A>T	NP_001166985.1:p.Asp39Val
NM_001173515.2:c.116A>T	NP_001166986.1:p.Asp39Val
NM_003332.4:c.149A>T MANE Select	NP_003323.1:p.Asp50Val
NM_198125.3:c.149A>T	NP_937758.1:p.Asp50Val
NR_033390.2:n.176A>T