Canonical Allele Identifier: CA1548128126

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56857454_56857455delinsCT , CM000667.2:g.56857454_56857455delinsCT	GRCh38
NC_000005.9:g.56153281_56153282delinsCT , CM000667.1:g.56153281_56153282delinsCT	GRCh37
NC_000005.8:g.56189038_56189039delinsCT	NCBI36
NG_031884.1:g.47382_47383delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.633+704_633+705delinsCT MANE Select	ENSP00000382423.3:n.633+704_633+705delinsCT
ENST00000399503.3:c.633+704_633+705delinsCT	ENSP00000382423.3:n.633+704_633+705delinsCT
NM_005921.1:c.633+704_633+705delinsCT	NP_005912.1:n.633+704_633+705delinsCT
XM_005248519.3:c.255+704_255+705delinsCT	XP_005248576.2:n.255+704_255+705delinsCT
XM_011543406.1:c.378+704_378+705delinsCT	XP_011541708.1:n.378+704_378+705delinsCT
XM_011543407.1:c.633+704_633+705delinsCT	XP_011541709.1:n.633+704_633+705delinsCT
XM_011543408.1:c.633+704_633+705delinsCT	XP_011541710.1:n.633+704_633+705delinsCT
XM_017009484.1:c.222+704_222+705delinsCT	XP_016864973.1:n.222+704_222+705delinsCT
XM_017009485.1:c.144+704_144+705delinsCT	XP_016864974.1:n.144+704_144+705delinsCT
XR_001742068.2:n.664+704_664+705delinsCT
NM_005921.2:c.633+704_633+705delinsCT MANE Select	NP_005912.1:n.633+704_633+705delinsCT