Canonical Allele Identifier: CA444399789

Gene: MAP3K1

Linked Data

• COSMIC: COSM1486855
• MyVariant Identifiers: chr5:g.56178144_56178145insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882317dup , CM000667.2:g.56882317dup	GRCh38
NC_000005.9:g.56178144dup , CM000667.1:g.56178144dup	GRCh37
NC_000005.8:g.56213901dup	NCBI36
NG_031884.1:g.72245dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3117dup MANE Select	ENSP00000382423.3:p.Asp1040ArgfsTer2
ENST00000399503.3:c.3117dup	ENSP00000382423.3:p.Asp1040ArgfsTer2
NM_005921.1:c.3117dup	NP_005912.1:p.Asp1040ArgfsTer2
XM_005248519.3:c.2739dup	XP_005248576.2:p.Asp914ArgfsTer2
XM_011543406.1:c.2862dup	XP_011541708.1:p.Asp955ArgfsTer2
XM_011543407.1:c.2838dup	XP_011541709.1:p.Asp947ArgfsTer2
XM_011543408.1:c.3117dup	XP_011541710.1:p.Asp1040ArgfsTer2
XM_017009484.1:c.2706dup	XP_016864973.1:p.Asp903ArgfsTer2
XM_017009485.1:c.2628dup	XP_016864974.1:p.Asp877ArgfsTer2
XR_001742068.2:n.3148dup
NM_005921.2:c.3117dup MANE Select	NP_005912.1:p.Asp1040ArgfsTer2