Canonical Allele Identifier: CA2766565217

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875442_56875449del , CM000667.2:g.56875442_56875449del	GRCh38
NC_000005.9:g.56171269_56171276del , CM000667.1:g.56171269_56171276del	GRCh37
NC_000005.8:g.56207026_56207033del	NCBI36
NG_031884.1:g.65370_65377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+132_1965+139del MANE Select	ENSP00000382423.3:n.1965+132_1965+139del
ENST00000399503.3:c.1965+132_1965+139del	ENSP00000382423.3:n.1965+132_1965+139del
NM_005921.1:c.1965+132_1965+139del	NP_005912.1:n.1965+132_1965+139del
XM_005248519.3:c.1587+132_1587+139del	XP_005248576.2:n.1587+132_1587+139del
XM_011543406.1:c.1710+132_1710+139del	XP_011541708.1:n.1710+132_1710+139del
XM_011543407.1:c.1686+2437_1686+2444del	XP_011541709.1:n.1686+2437_1686+2444del
XM_011543408.1:c.1965+132_1965+139del	XP_011541710.1:n.1965+132_1965+139del
XM_017009484.1:c.1554+132_1554+139del	XP_016864973.1:n.1554+132_1554+139del
XM_017009485.1:c.1476+132_1476+139del	XP_016864974.1:n.1476+132_1476+139del
XR_001742068.2:n.1996+132_1996+139del
NM_005921.2:c.1965+132_1965+139del MANE Select	NP_005912.1:n.1965+132_1965+139del