Canonical Allele Identifier: CA2673909450

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56875400-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875403del , CM000667.2:g.56875403del	GRCh38
NC_000005.9:g.56171230del , CM000667.1:g.56171230del	GRCh37
NC_000005.8:g.56206987del	NCBI36
NG_031884.1:g.65331del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+93del MANE Select	ENSP00000382423.3:n.1965+93del
ENST00000399503.3:c.1965+93del	ENSP00000382423.3:n.1965+93del
NM_005921.1:c.1965+93del	NP_005912.1:n.1965+93del
XM_005248519.3:c.1587+93del	XP_005248576.2:n.1587+93del
XM_011543406.1:c.1710+93del	XP_011541708.1:n.1710+93del
XM_011543407.1:c.1686+2398del	XP_011541709.1:n.1686+2398del
XM_011543408.1:c.1965+93del	XP_011541710.1:n.1965+93del
XM_017009484.1:c.1554+93del	XP_016864973.1:n.1554+93del
XM_017009485.1:c.1476+93del	XP_016864974.1:n.1476+93del
XR_001742068.2:n.1996+93del
NM_005921.2:c.1965+93del MANE Select	NP_005912.1:n.1965+93del