Canonical Allele Identifier: CA444399763

Gene: MAP3K1

Linked Data

• COSMIC: COSM1486853
• MyVariant Identifiers: chr5:g.56178136_56178137insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882311dup , CM000667.2:g.56882311dup	GRCh38
NC_000005.9:g.56178138dup , CM000667.1:g.56178138dup	GRCh37
NC_000005.8:g.56213895dup	NCBI36
NG_031884.1:g.72239dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3111dup MANE Select	ENSP00000382423.3:p.Asp1038ArgfsTer4
ENST00000399503.3:c.3111dup	ENSP00000382423.3:p.Asp1038ArgfsTer4
NM_005921.1:c.3111dup	NP_005912.1:p.Asp1038ArgfsTer4
XM_005248519.3:c.2733dup	XP_005248576.2:p.Asp912ArgfsTer4
XM_011543406.1:c.2856dup	XP_011541708.1:p.Asp953ArgfsTer4
XM_011543407.1:c.2832dup	XP_011541709.1:p.Asp945ArgfsTer4
XM_011543408.1:c.3111dup	XP_011541710.1:p.Asp1038ArgfsTer4
XM_017009484.1:c.2700dup	XP_016864973.1:p.Asp901ArgfsTer4
XM_017009485.1:c.2622dup	XP_016864974.1:p.Asp875ArgfsTer4
XR_001742068.2:n.3142dup
NM_005921.2:c.3111dup MANE Select	NP_005912.1:p.Asp1038ArgfsTer4