Canonical Allele Identifier: CA645557025

Gene: MAP3K1

Linked Data

• COSMIC: COSM5029160

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882264_56882265del , CM000667.2:g.56882264_56882265del	GRCh38
NC_000005.9:g.56178091_56178092del , CM000667.1:g.56178091_56178092del	GRCh37
NC_000005.8:g.56213848_56213849del	NCBI36
NG_031884.1:g.72192_72193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3064_3065del MANE Select	ENSP00000382423.3:p.Gln1022AlafsTer13
ENST00000399503.3:c.3064_3065del	ENSP00000382423.3:p.Gln1022AlafsTer13
NM_005921.1:c.3064_3065del	NP_005912.1:p.Gln1022AlafsTer13
XM_005248519.3:c.2686_2687del	XP_005248576.2:p.Gln896AlafsTer13
XM_011543406.1:c.2809_2810del	XP_011541708.1:p.Gln937AlafsTer13
XM_011543407.1:c.2785_2786del	XP_011541709.1:p.Gln929AlafsTer13
XM_011543408.1:c.3064_3065del	XP_011541710.1:p.Gln1022AlafsTer13
XM_017009484.1:c.2653_2654del	XP_016864973.1:p.Gln885AlafsTer13
XM_017009485.1:c.2575_2576del	XP_016864974.1:p.Gln859AlafsTer13
XR_001742068.2:n.3095_3096del
NM_005921.2:c.3064_3065del MANE Select	NP_005912.1:p.Gln1022AlafsTer13