Canonical Allele Identifier: CA444399796

Gene: MAP3K1

Linked Data

• COSMIC: COSM449857
• MyVariant Identifiers: chr5:g.56178146del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882319del , CM000667.2:g.56882319del	GRCh38
NC_000005.9:g.56178146del , CM000667.1:g.56178146del	GRCh37
NC_000005.8:g.56213903del	NCBI36
NG_031884.1:g.72247del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3119del MANE Select	ENSP00000382423.3:p.Asp1040ValfsTer?
ENST00000399503.3:c.3119del	ENSP00000382423.3:p.Asp1040ValfsTer?
NM_005921.1:c.3119del	NP_005912.1:p.Asp1040ValfsTer?
XM_005248519.3:c.2741del	XP_005248576.2:p.Asp914ValfsTer?
XM_011543406.1:c.2864del	XP_011541708.1:p.Asp955ValfsTer?
XM_011543407.1:c.2840del	XP_011541709.1:p.Asp947ValfsTer?
XM_011543408.1:c.3119del	XP_011541710.1:p.Asp1040ValfsTer?
XM_017009484.1:c.2708del	XP_016864973.1:p.Asp903ValfsTer?
XM_017009485.1:c.2630del	XP_016864974.1:p.Asp877ValfsTer?
XR_001742068.2:n.3150del
NM_005921.2:c.3119del MANE Select	NP_005912.1:p.Asp1040ValfsTer?