Canonical Allele Identifier: CA1548129295
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859970T= , CM000667.2:g.56859970T= GRCh38
NC_000005.9:g.56155797T= , CM000667.1:g.56155797T= GRCh37
NC_000005.8:g.56191554T= NCBI36
NG_031884.1:g.49898T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.834+55T= MANE Select ENSP00000382423.3:n.834+55T=
ENST00000399503.3:c.834+55T= ENSP00000382423.3:n.834+55T=
NM_005921.1:c.834+55T= NP_005912.1:n.834+55T=
XM_005248519.3:c.456+55T= XP_005248576.2:n.456+55T=
XM_011543406.1:c.579+55T= XP_011541708.1:n.579+55T=
XM_011543407.1:c.834+55T= XP_011541709.1:n.834+55T=
XM_011543408.1:c.834+55T= XP_011541710.1:n.834+55T=
XM_017009484.1:c.423+55T= XP_016864973.1:n.423+55T=
XM_017009485.1:c.345+55T= XP_016864974.1:n.345+55T=
XR_001742068.2:n.865+55T=
NM_005921.2:c.834+55T= MANE Select NP_005912.1:n.834+55T=