Canonical Allele Identifier: CA9393117

Gene: TYROBP

Linked Data

• dbSNP Id: rs750536324
• ExAC: 19:36398531 G / GA
• gnomAD v2: 19-36398531-G-GA
• gnomAD v3: 19-35907629-G-GA
• gnomAD v4: 19-35907629-G-GA
• MyVariant Identifiers: chr19:g.36398532_36398533insA (hg19) ; chr19:g.36398531_36398532insA (hg19) ; chr19:g.35907629_35907630insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35907630dup , CM000681.2:g.35907630dup	GRCh38
NC_000019.9:g.36398532dup , CM000681.1:g.36398532dup	GRCh37
NC_000019.8:g.41090372dup	NCBI36
NG_009304.1:g.5655dup , LRG_607:g.5655dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262629.9:c.95-50dup MANE Select	ENSP00000262629.3:n.95-50dup
ENST00000262629.8:c.95-50dup	ENSP00000262629.3:n.95-50dup
ENST00000424586.7:c.62-50dup	ENSP00000402371.3:n.62-50dup
ENST00000544690.6:c.62-50dup	ENSP00000445332.1:n.62-50dup
ENST00000585626.1:n.162-50dup
ENST00000585901.6:c.95-50dup	ENSP00000468608.1:n.95-50dup
ENST00000586946.1:c.88-50dup	ENSP00000465656.1:n.88-50dup
ENST00000587837.5:c.88-50dup	ENSP00000465081.1:n.88-50dup
ENST00000588439.1:n.189dup
ENST00000589517.1:c.95-50dup	ENSP00000468447.1:n.95-50dup
NM_001173514.1:c.62-50dup	NP_001166985.1:n.62-50dup
NM_001173515.1:c.62-50dup	NP_001166986.1:n.62-50dup
NM_003332.3:c.95-50dup , LRG_607t1:c.95-50dup	NP_003323.1:n.95-50dup
NM_198125.2:c.95-50dup	NP_937758.1:n.95-50dup
NR_033390.1:n.136-50dup
NM_001173514.2:c.62-50dup	NP_001166985.1:n.62-50dup
NM_001173515.2:c.62-50dup	NP_001166986.1:n.62-50dup
NM_003332.4:c.95-50dup MANE Select	NP_003323.1:n.95-50dup
NM_198125.3:c.95-50dup	NP_937758.1:n.95-50dup
NR_033390.2:n.122-50dup