Canonical Allele Identifier: CA2673908391

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56859995-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859996del , CM000667.2:g.56859996del	GRCh38
NC_000005.9:g.56155823del , CM000667.1:g.56155823del	GRCh37
NC_000005.8:g.56191580del	NCBI36
NG_031884.1:g.49924del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.834+81del MANE Select	ENSP00000382423.3:n.834+81del
ENST00000399503.3:c.834+81del	ENSP00000382423.3:n.834+81del
NM_005921.1:c.834+81del	NP_005912.1:n.834+81del
XM_005248519.3:c.456+81del	XP_005248576.2:n.456+81del
XM_011543406.1:c.579+81del	XP_011541708.1:n.579+81del
XM_011543407.1:c.834+81del	XP_011541709.1:n.834+81del
XM_011543408.1:c.834+81del	XP_011541710.1:n.834+81del
XM_017009484.1:c.423+81del	XP_016864973.1:n.423+81del
XM_017009485.1:c.345+81del	XP_016864974.1:n.345+81del
XR_001742068.2:n.865+81del
NM_005921.2:c.834+81del MANE Select	NP_005912.1:n.834+81del