Canonical Allele Identifier: CA2673908403

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56860013-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56860014_56860015dup , CM000667.2:g.56860014_56860015dup	GRCh38
NC_000005.9:g.56155841_56155842dup , CM000667.1:g.56155841_56155842dup	GRCh37
NC_000005.8:g.56191598_56191599dup	NCBI36
NG_031884.1:g.49942_49943dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.834+99_834+100dup MANE Select	ENSP00000382423.3:n.834+99_834+100dup
ENST00000399503.3:c.834+99_834+100dup	ENSP00000382423.3:n.834+99_834+100dup
NM_005921.1:c.834+99_834+100dup	NP_005912.1:n.834+99_834+100dup
XM_005248519.3:c.456+99_456+100dup	XP_005248576.2:n.456+99_456+100dup
XM_011543406.1:c.579+99_579+100dup	XP_011541708.1:n.579+99_579+100dup
XM_011543407.1:c.834+99_834+100dup	XP_011541709.1:n.834+99_834+100dup
XM_011543408.1:c.834+99_834+100dup	XP_011541710.1:n.834+99_834+100dup
XM_017009484.1:c.423+99_423+100dup	XP_016864973.1:n.423+99_423+100dup
XM_017009485.1:c.345+99_345+100dup	XP_016864974.1:n.345+99_345+100dup
XR_001742068.2:n.865+99_865+100dup
NM_005921.2:c.834+99_834+100dup MANE Select	NP_005912.1:n.834+99_834+100dup