Canonical Allele Identifier: CA405388052

Gene: TYROBP

Linked Data

• MyVariant Identifiers: chr19:g.36398405C>T (hg19) ; chr19:g.35907503C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907503C>T , CM000681.2:g.35907503C>T	GRCh38
NC_000019.9:g.36398405C>T , CM000681.1:g.36398405C>T	GRCh37
NC_000019.8:g.41090245C>T	NCBI36
NG_009304.1:g.5782G>A , LRG_607:g.5782G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.172G>A MANE Select	ENSP00000262629.3:p.Ala58Thr
ENST00000262629.8:c.172G>A	ENSP00000262629.3:p.Ala58Thr
ENST00000424586.7:c.139G>A	ENSP00000402371.3:p.Ala47Thr
ENST00000544690.6:c.139G>A	ENSP00000445332.1:p.Ala47Thr
ENST00000585626.1:n.239G>A
ENST00000585901.6:c.172G>A	ENSP00000468608.1:p.Ala58Thr
ENST00000586946.1:c.*57G>A	ENSP00000465656.1:n.*57G>A
ENST00000587837.5:c.*57G>A	ENSP00000465081.1:n.*57G>A
ENST00000588439.1:n.316G>A
ENST00000589517.1:c.172G>A	ENSP00000468447.1:p.Ala58Thr
NM_001173514.1:c.139G>A	NP_001166985.1:p.Ala47Thr
NM_001173515.1:c.139G>A	NP_001166986.1:p.Ala47Thr
NM_003332.3:c.172G>A , LRG_607t1:c.172G>A	NP_003323.1:p.Ala58Thr
NM_198125.2:c.172G>A	NP_937758.1:p.Ala58Thr
NR_033390.1:n.213G>A
NM_001173514.2:c.139G>A	NP_001166985.1:p.Ala47Thr
NM_001173515.2:c.139G>A	NP_001166986.1:p.Ala47Thr
NM_003332.4:c.172G>A MANE Select	NP_003323.1:p.Ala58Thr
NM_198125.3:c.172G>A	NP_937758.1:p.Ala58Thr
NR_033390.2:n.199G>A