Canonical Allele Identifier: CA1548128152

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56857509_56857510delinsCA , CM000667.2:g.56857509_56857510delinsCA	GRCh38
NC_000005.9:g.56153336_56153337delinsCA , CM000667.1:g.56153336_56153337delinsCA	GRCh37
NC_000005.8:g.56189093_56189094delinsCA	NCBI36
NG_031884.1:g.47437_47438delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.633+759_633+760delinsCA MANE Select	ENSP00000382423.3:n.633+759_633+760delins...
ENST00000399503.3:c.633+759_633+760delinsCA	ENSP00000382423.3:n.633+759_633+760delins...
NM_005921.1:c.633+759_633+760delinsCA	NP_005912.1:n.633+759_633+760delinsCA
XM_005248519.3:c.255+759_255+760delinsCA	XP_005248576.2:n.255+759_255+760delinsCA
XM_011543406.1:c.378+759_378+760delinsCA	XP_011541708.1:n.378+759_378+760delinsCA
XM_011543407.1:c.633+759_633+760delinsCA	XP_011541709.1:n.633+759_633+760delinsCA
XM_011543408.1:c.633+759_633+760delinsCA	XP_011541710.1:n.633+759_633+760delinsCA
XM_017009484.1:c.222+759_222+760delinsCA	XP_016864973.1:n.222+759_222+760delinsCA
XM_017009485.1:c.144+759_144+760delinsCA	XP_016864974.1:n.144+759_144+760delinsCA
XR_001742068.2:n.664+759_664+760delinsCA
NM_005921.2:c.633+759_633+760delinsCA MANE Select	NP_005912.1:n.633+759_633+760delinsCA