Canonical Allele Identifier: CA2673909477

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56875446-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875448del , CM000667.2:g.56875448del	GRCh38
NC_000005.9:g.56171275del , CM000667.1:g.56171275del	GRCh37
NC_000005.8:g.56207032del	NCBI36
NG_031884.1:g.65376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+138del MANE Select	ENSP00000382423.3:n.1965+138del
ENST00000399503.3:c.1965+138del	ENSP00000382423.3:n.1965+138del
NM_005921.1:c.1965+138del	NP_005912.1:n.1965+138del
XM_005248519.3:c.1587+138del	XP_005248576.2:n.1587+138del
XM_011543406.1:c.1710+138del	XP_011541708.1:n.1710+138del
XM_011543407.1:c.1686+2443del	XP_011541709.1:n.1686+2443del
XM_011543408.1:c.1965+138del	XP_011541710.1:n.1965+138del
XM_017009484.1:c.1554+138del	XP_016864973.1:n.1554+138del
XM_017009485.1:c.1476+138del	XP_016864974.1:n.1476+138del
XR_001742068.2:n.1996+138del
NM_005921.2:c.1965+138del MANE Select	NP_005912.1:n.1965+138del