Canonical Allele Identifier: CA2766565148

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56857483_56857485del , CM000667.2:g.56857483_56857485del	GRCh38
NC_000005.9:g.56153310_56153312del , CM000667.1:g.56153310_56153312del	GRCh37
NC_000005.8:g.56189067_56189069del	NCBI36
NG_031884.1:g.47411_47413del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.633+733_633+735del MANE Select	ENSP00000382423.3:n.633+733_633+735del
ENST00000399503.3:c.633+733_633+735del	ENSP00000382423.3:n.633+733_633+735del
NM_005921.1:c.633+733_633+735del	NP_005912.1:n.633+733_633+735del
XM_005248519.3:c.255+733_255+735del	XP_005248576.2:n.255+733_255+735del
XM_011543406.1:c.378+733_378+735del	XP_011541708.1:n.378+733_378+735del
XM_011543407.1:c.633+733_633+735del	XP_011541709.1:n.633+733_633+735del
XM_011543408.1:c.633+733_633+735del	XP_011541710.1:n.633+733_633+735del
XM_017009484.1:c.222+733_222+735del	XP_016864973.1:n.222+733_222+735del
XM_017009485.1:c.144+733_144+735del	XP_016864974.1:n.144+733_144+735del
XR_001742068.2:n.664+733_664+735del
NM_005921.2:c.633+733_633+735del MANE Select	NP_005912.1:n.633+733_633+735del