Canonical Allele Identifier: CA1076362679

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1747443390
• gnomAD v3: 5-56859665-TTACC-T
• gnomAD v4: 5-56859665-TTACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859667_56859670del , CM000667.2:g.56859667_56859670del	GRCh38
NC_000005.9:g.56155494_56155497del , CM000667.1:g.56155494_56155497del	GRCh37
NC_000005.8:g.56191251_56191254del	NCBI36
NG_031884.1:g.49595_49598del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.634-48_634-45del MANE Select	ENSP00000382423.3:n.634-48_634-45del
ENST00000399503.3:c.634-48_634-45del	ENSP00000382423.3:n.634-48_634-45del
NM_005921.1:c.634-48_634-45del	NP_005912.1:n.634-48_634-45del
XM_005248519.3:c.256-48_256-45del	XP_005248576.2:n.256-48_256-45del
XM_011543406.1:c.379-48_379-45del	XP_011541708.1:n.379-48_379-45del
XM_011543407.1:c.634-48_634-45del	XP_011541709.1:n.634-48_634-45del
XM_011543408.1:c.634-48_634-45del	XP_011541710.1:n.634-48_634-45del
XM_017009484.1:c.223-48_223-45del	XP_016864973.1:n.223-48_223-45del
XM_017009485.1:c.145-48_145-45del	XP_016864974.1:n.145-48_145-45del
XR_001742068.2:n.665-48_665-45del
NM_005921.2:c.634-48_634-45del MANE Select	NP_005912.1:n.634-48_634-45del