Canonical Allele Identifier: CA1548139550
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882310_56882316delinsAAGACTC , CM000667.2:g.56882310_56882316delinsAAGACTC GRCh38
NC_000005.9:g.56178137_56178143delinsAAGACTC , CM000667.1:g.56178137_56178143delinsAAGACTC GRCh37
NC_000005.8:g.56213894_56213900delinsAAGACTC NCBI36
NG_031884.1:g.72238_72244delinsAAGACTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3110_3116delinsAAGACTC MANE Select ENSP00000382423.3:p.Lys1037=
ENST00000399503.3:c.3110_3116delinsAAGACTC ENSP00000382423.3:p.Lys1037=
NM_005921.1:c.3110_3116delinsAAGACTC NP_005912.1:p.Lys1037=
XM_005248519.3:c.2732_2738delinsAAGACTC XP_005248576.2:p.Lys911=
XM_011543406.1:c.2855_2861delinsAAGACTC XP_011541708.1:p.Lys952=
XM_011543407.1:c.2831_2837delinsAAGACTC XP_011541709.1:p.Lys944=
XM_011543408.1:c.3110_3116delinsAAGACTC XP_011541710.1:p.Lys1037=
XM_017009484.1:c.2699_2705delinsAAGACTC XP_016864973.1:p.Lys900=
XM_017009485.1:c.2621_2627delinsAAGACTC XP_016864974.1:p.Lys874=
XR_001742068.2:n.3141_3147delinsAAGACTC
NM_005921.2:c.3110_3116delinsAAGACTC MANE Select NP_005912.1:p.Lys1037=