Canonical Allele Identifier: CA353277592

Gene: TASOR

Linked Data

• ClinVar Variation Id: 487784
• ClinVar RCV Id: RCV000577835
• dbSNP Id: rs1553733337
• MyVariant Identifiers: chr3:g.56716938C>T (hg19) ; chr3:g.56682910C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.56682910C>T , CM000665.2:g.56682910C>T	GRCh38
NC_000003.11:g.56716938C>T , CM000665.1:g.56716938C>T	GRCh37
NC_000003.10:g.56691978C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683822.1:c.97G>A MANE Select	ENSP00000508241.1:p.Glu33Lys
ENST00000355628.9:c.97G>A	ENSP00000347845.5:p.Glu33Lys
ENST00000493960.6:c.97G>A	ENSP00000417509.2:p.Glu33Lys
NM_001112736.1:c.97G>A	NP_001106207.1:p.Glu33Lys
XM_005264999.1:c.97G>A	XP_005265056.1:p.Glu33Lys
XM_006713077.1:c.97G>A	XP_006713140.1:p.Glu33Lys
XM_011533552.1:c.97G>A	XP_011531854.1:p.Glu33Lys
NM_001363940.1:c.97G>A	NP_001350869.1:p.Glu33Lys
NM_001365635.1:c.97G>A	NP_001352564.1:p.Glu33Lys
NM_001365636.1:c.97G>A	NP_001352565.1:p.Glu33Lys
NM_001365637.1:c.97G>A	NP_001352566.1:p.Glu33Lys
NM_001365638.1:c.97G>A	NP_001352567.1:p.Glu33Lys
NM_001112736.2:c.97G>A	NP_001106207.1:p.Glu33Lys
NM_001365635.2:c.97G>A MANE Select	NP_001352564.1:p.Glu33Lys
NM_001365636.2:c.97G>A	NP_001352565.1:p.Glu33Lys
NM_001365637.2:c.97G>A	NP_001352566.1:p.Glu33Lys
NM_001365638.2:c.97G>A	NP_001352567.1:p.Glu33Lys