Canonical Allele Identifier: CA2673909979

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56882021-T-TCAACAACAA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882039_56882047dup , CM000667.2:g.56882039_56882047dup	GRCh38
NC_000005.9:g.56177866_56177874dup , CM000667.1:g.56177866_56177874dup	GRCh37
NC_000005.8:g.56213623_56213631dup	NCBI36
NG_031884.1:g.71967_71975dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2839_2847dup MANE Select	ENSP00000382423.3:p.Thr949_Glu950insThrThrThr
ENST00000399503.3:c.2839_2847dup	ENSP00000382423.3:p.Thr949_Glu950insThrThrThr
NM_005921.1:c.2839_2847dup	NP_005912.1:p.Thr949_Glu950insThrThrThr
XM_005248519.3:c.2461_2469dup	XP_005248576.2:p.Thr823_Glu824insThrThrThr
XM_011543406.1:c.2584_2592dup	XP_011541708.1:p.Thr864_Glu865insThrThrThr
XM_011543407.1:c.2560_2568dup	XP_011541709.1:p.Thr856_Glu857insThrThrThr
XM_011543408.1:c.2839_2847dup	XP_011541710.1:p.Thr949_Glu950insThrThrThr
XM_017009484.1:c.2428_2436dup	XP_016864973.1:p.Thr812_Glu813insThrThrThr
XM_017009485.1:c.2350_2358dup	XP_016864974.1:p.Thr786_Glu787insThrThrThr
XR_001742068.2:n.2870_2878dup
NM_005921.2:c.2839_2847dup MANE Select	NP_005912.1:p.Thr949_Glu950insThrThrThr