Canonical Allele Identifier: CA444399691

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1160803088
• gnomAD v4: 5-56882290-C-T
• MyVariant Identifiers: chr5:g.56178117C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882290C>T , CM000667.2:g.56882290C>T	GRCh38
NC_000005.9:g.56178117C>T , CM000667.1:g.56178117C>T	GRCh37
NC_000005.8:g.56213874C>T	NCBI36
NG_031884.1:g.72218C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3090C>T MANE Select	ENSP00000382423.3:p.His1030=
ENST00000399503.3:c.3090C>T	ENSP00000382423.3:p.His1030=
NM_005921.1:c.3090C>T	NP_005912.1:p.His1030=
XM_005248519.3:c.2712C>T	XP_005248576.2:p.His904=
XM_011543406.1:c.2835C>T	XP_011541708.1:p.His945=
XM_011543407.1:c.2811C>T	XP_011541709.1:p.His937=
XM_011543408.1:c.3090C>T	XP_011541710.1:p.His1030=
XM_017009484.1:c.2679C>T	XP_016864973.1:p.His893=
XM_017009485.1:c.2601C>T	XP_016864974.1:p.His867=
XR_001742068.2:n.3121C>T
NM_005921.2:c.3090C>T MANE Select	NP_005912.1:p.His1030=