Canonical Allele Identifier: CA1548136585

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875578_56875580delinsGAA , CM000667.2:g.56875578_56875580delinsGAA	GRCh38
NC_000005.9:g.56171405_56171407delinsGAA , CM000667.1:g.56171405_56171407delinsGAA	GRCh37
NC_000005.8:g.56207162_56207164delinsGAA	NCBI36
NG_031884.1:g.65506_65508delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+268_1965+270delinsGAA MANE Select	ENSP00000382423.3:n.1965+268_1965+270delinsGAA
ENST00000399503.3:c.1965+268_1965+270delinsGAA	ENSP00000382423.3:n.1965+268_1965+270delinsGAA
NM_005921.1:c.1965+268_1965+270delinsGAA	NP_005912.1:n.1965+268_1965+270delinsGAA
XM_005248519.3:c.1587+268_1587+270delinsGAA	XP_005248576.2:n.1587+268_1587+270delinsGAA
XM_011543406.1:c.1710+268_1710+270delinsGAA	XP_011541708.1:n.1710+268_1710+270delinsGAA
XM_011543407.1:c.1686+2573_1686+2575delinsGAA	XP_011541709.1:n.1686+2573_1686+2575delinsGAA
XM_011543408.1:c.1965+268_1965+270delinsGAA	XP_011541710.1:n.1965+268_1965+270delinsGAA
XM_017009484.1:c.1554+268_1554+270delinsGAA	XP_016864973.1:n.1554+268_1554+270delinsGAA
XM_017009485.1:c.1476+268_1476+270delinsGAA	XP_016864974.1:n.1476+268_1476+270delinsGAA
XR_001742068.2:n.1996+268_1996+270delinsGAA
NM_005921.2:c.1965+268_1965+270delinsGAA MANE Select	NP_005912.1:n.1965+268_1965+270delinsGAA