Canonical Allele Identifier: CA2708985401

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111943340

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882035_56882036insCCAACA , CM000667.2:g.56882035_56882036insCCAACA	GRCh38
NC_000005.9:g.56177862_56177863insCCAACA , CM000667.1:g.56177862_56177863insCCAACA	GRCh37
NC_000005.8:g.56213619_56213620insCCAACA	NCBI36
NG_031884.1:g.71963_71964insCCAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2835_2836insCCAACA MANE Select	ENSP00000382423.3:p.Thr945_Thr946insProThr
ENST00000399503.3:c.2835_2836insCCAACA	ENSP00000382423.3:p.Thr945_Thr946insProThr
NM_005921.1:c.2835_2836insCCAACA	NP_005912.1:p.Thr945_Thr946insProThr
XM_005248519.3:c.2457_2458insCCAACA	XP_005248576.2:p.Thr819_Thr820insProThr
XM_011543406.1:c.2580_2581insCCAACA	XP_011541708.1:p.Thr860_Thr861insProThr
XM_011543407.1:c.2556_2557insCCAACA	XP_011541709.1:p.Thr852_Thr853insProThr
XM_011543408.1:c.2835_2836insCCAACA	XP_011541710.1:p.Thr945_Thr946insProThr
XM_017009484.1:c.2424_2425insCCAACA	XP_016864973.1:p.Thr808_Thr809insProThr
XM_017009485.1:c.2346_2347insCCAACA	XP_016864974.1:p.Thr782_Thr783insProThr
XR_001742068.2:n.2866_2867insCCAACA
NM_005921.2:c.2835_2836insCCAACA MANE Select	NP_005912.1:p.Thr945_Thr946insProThr