Canonical Allele Identifier: CA2673908386
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859989dup , CM000667.2:g.56859989dup GRCh38
NC_000005.9:g.56155816dup , CM000667.1:g.56155816dup GRCh37
NC_000005.8:g.56191573dup NCBI36
NG_031884.1:g.49917dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.834+74dup MANE Select ENSP00000382423.3:n.834+74dup
ENST00000399503.3:c.834+74dup ENSP00000382423.3:n.834+74dup
NM_005921.1:c.834+74dup NP_005912.1:n.834+74dup
XM_005248519.3:c.456+74dup XP_005248576.2:n.456+74dup
XM_011543406.1:c.579+74dup XP_011541708.1:n.579+74dup
XM_011543407.1:c.834+74dup XP_011541709.1:n.834+74dup
XM_011543408.1:c.834+74dup XP_011541710.1:n.834+74dup
XM_017009484.1:c.423+74dup XP_016864973.1:n.423+74dup
XM_017009485.1:c.345+74dup XP_016864974.1:n.345+74dup
XR_001742068.2:n.865+74dup
NM_005921.2:c.834+74dup MANE Select NP_005912.1:n.834+74dup