Canonical Allele Identifier: CA2766565209

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875360_56875382del , CM000667.2:g.56875360_56875382del	GRCh38
NC_000005.9:g.56171187_56171209del , CM000667.1:g.56171187_56171209del	GRCh37
NC_000005.8:g.56206944_56206966del	NCBI36
NG_031884.1:g.65288_65310del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+50_1965+72del MANE Select	ENSP00000382423.3:n.1965+50_1965+72del
ENST00000399503.3:c.1965+50_1965+72del	ENSP00000382423.3:n.1965+50_1965+72del
NM_005921.1:c.1965+50_1965+72del	NP_005912.1:n.1965+50_1965+72del
XM_005248519.3:c.1587+50_1587+72del	XP_005248576.2:n.1587+50_1587+72del
XM_011543406.1:c.1710+50_1710+72del	XP_011541708.1:n.1710+50_1710+72del
XM_011543407.1:c.1686+2355_1686+2377del	XP_011541709.1:n.1686+2355_1686+2377del
XM_011543408.1:c.1965+50_1965+72del	XP_011541710.1:n.1965+50_1965+72del
XM_017009484.1:c.1554+50_1554+72del	XP_016864973.1:n.1554+50_1554+72del
XM_017009485.1:c.1476+50_1476+72del	XP_016864974.1:n.1476+50_1476+72del
XR_001742068.2:n.1996+50_1996+72del
NM_005921.2:c.1965+50_1965+72del MANE Select	NP_005912.1:n.1965+50_1965+72del