Canonical Allele Identifier: CA444399166

Gene: MAP3K1

Linked Data

• COSMIC: COSM449845
• MyVariant Identifiers: chr5:g.56177598del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881772del , CM000667.2:g.56881772del	GRCh38
NC_000005.9:g.56177599del , CM000667.1:g.56177599del	GRCh37
NC_000005.8:g.56213356del	NCBI36
NG_031884.1:g.71700del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2572del MANE Select	ENSP00000382423.3:p.Ala858LeufsTer16
ENST00000399503.3:c.2572del	ENSP00000382423.3:p.Ala858LeufsTer16
NM_005921.1:c.2572del	NP_005912.1:p.Ala858LeufsTer16
XM_005248519.3:c.2194del	XP_005248576.2:p.Ala732LeufsTer16
XM_011543406.1:c.2317del	XP_011541708.1:p.Ala773LeufsTer16
XM_011543407.1:c.2293del	XP_011541709.1:p.Ala765LeufsTer16
XM_011543408.1:c.2572del	XP_011541710.1:p.Ala858LeufsTer16
XM_017009484.1:c.2161del	XP_016864973.1:p.Ala721LeufsTer16
XM_017009485.1:c.2083del	XP_016864974.1:p.Ala695LeufsTer16
XR_001742068.2:n.2603del
NM_005921.2:c.2572del MANE Select	NP_005912.1:p.Ala858LeufsTer16