Canonical Allele Identifier: CA2708985477

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111943456

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882046_56882048del , CM000667.2:g.56882046_56882048del	GRCh38
NC_000005.9:g.56177873_56177875del , CM000667.1:g.56177873_56177875del	GRCh37
NC_000005.8:g.56213630_56213632del	NCBI36
NG_031884.1:g.71974_71976del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2846_2848del MANE Select	ENSP00000382423.3:p.Thr949_Glu950delinsLys
ENST00000399503.3:c.2846_2848del	ENSP00000382423.3:p.Thr949_Glu950delinsLys
NM_005921.1:c.2846_2848del	NP_005912.1:p.Thr949_Glu950delinsLys
XM_005248519.3:c.2468_2470del	XP_005248576.2:p.Thr823_Glu824delinsLys
XM_011543406.1:c.2591_2593del	XP_011541708.1:p.Thr864_Glu865delinsLys
XM_011543407.1:c.2567_2569del	XP_011541709.1:p.Thr856_Glu857delinsLys
XM_011543408.1:c.2846_2848del	XP_011541710.1:p.Thr949_Glu950delinsLys
XM_017009484.1:c.2435_2437del	XP_016864973.1:p.Thr812_Glu813delinsLys
XM_017009485.1:c.2357_2359del	XP_016864974.1:p.Thr786_Glu787delinsLys
XR_001742068.2:n.2877_2879del
NM_005921.2:c.2846_2848del MANE Select	NP_005912.1:p.Thr949_Glu950delinsLys