Canonical Allele Identifier: CA444399878

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111946012
• MyVariant Identifiers: chr5:g.56178168T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882341T>G , CM000667.2:g.56882341T>G	GRCh38
NC_000005.9:g.56178168T>G , CM000667.1:g.56178168T>G	GRCh37
NC_000005.8:g.56213925T>G	NCBI36
NG_031884.1:g.72269T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3141T>G MANE Select	ENSP00000382423.3:p.Thr1047=
ENST00000399503.3:c.3141T>G	ENSP00000382423.3:p.Thr1047=
NM_005921.1:c.3141T>G	NP_005912.1:p.Thr1047=
XM_005248519.3:c.2763T>G	XP_005248576.2:p.Thr921=
XM_011543406.1:c.2886T>G	XP_011541708.1:p.Thr962=
XM_011543407.1:c.2862T>G	XP_011541709.1:p.Thr954=
XM_011543408.1:c.3141T>G	XP_011541710.1:p.Thr1047=
XM_017009484.1:c.2730T>G	XP_016864973.1:p.Thr910=
XM_017009485.1:c.2652T>G	XP_016864974.1:p.Thr884=
XR_001742068.2:n.3172T>G
NM_005921.2:c.3141T>G MANE Select	NP_005912.1:p.Thr1047=