Canonical Allele Identifier: CA444399905

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178177A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882350A>G , CM000667.2:g.56882350A>G	GRCh38
NC_000005.9:g.56178177A>G , CM000667.1:g.56178177A>G	GRCh37
NC_000005.8:g.56213934A>G	NCBI36
NG_031884.1:g.72278A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3150A>G MANE Select	ENSP00000382423.3:p.Arg1050=
ENST00000399503.3:c.3150A>G	ENSP00000382423.3:p.Arg1050=
NM_005921.1:c.3150A>G	NP_005912.1:p.Arg1050=
XM_005248519.3:c.2772A>G	XP_005248576.2:p.Arg924=
XM_011543406.1:c.2895A>G	XP_011541708.1:p.Arg965=
XM_011543407.1:c.2871A>G	XP_011541709.1:p.Arg957=
XM_011543408.1:c.3150A>G	XP_011541710.1:p.Arg1050=
XM_017009484.1:c.2739A>G	XP_016864973.1:p.Arg913=
XM_017009485.1:c.2661A>G	XP_016864974.1:p.Arg887=
XR_001742068.2:n.3181A>G
NM_005921.2:c.3150A>G MANE Select	NP_005912.1:p.Arg1050=