Canonical Allele Identifier: CA3272572

Gene: MAP3K1

Linked Data

• dbSNP Id: rs772105702
• ExAC: 5:56155494 AC / A
• gnomAD v2: 5-56155494-AC-A
• gnomAD v3: 5-56859667-AC-A
• gnomAD v4: 5-56859667-AC-A
• MyVariant Identifiers: chr5:g.56155495del (hg19) ; chr5:g.56859668del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859669del , CM000667.2:g.56859669del	GRCh38
NC_000005.9:g.56155496del , CM000667.1:g.56155496del	GRCh37
NC_000005.8:g.56191253del	NCBI36
NG_031884.1:g.49597del

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.634-46del MANE Select	ENSP00000382423.3:n.634-46del
ENST00000399503.3:c.634-46del	ENSP00000382423.3:n.634-46del
NM_005921.1:c.634-46del	NP_005912.1:n.634-46del
XM_005248519.3:c.256-46del	XP_005248576.2:n.256-46del
XM_011543406.1:c.379-46del	XP_011541708.1:n.379-46del
XM_011543407.1:c.634-46del	XP_011541709.1:n.634-46del
XM_011543408.1:c.634-46del	XP_011541710.1:n.634-46del
XM_017009484.1:c.223-46del	XP_016864973.1:n.223-46del
XM_017009485.1:c.145-46del	XP_016864974.1:n.145-46del
XR_001742068.2:n.665-46del
NM_005921.2:c.634-46del MANE Select	NP_005912.1:n.634-46del