Canonical Allele Identifier: CA444398898

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56170927G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875100G>A , CM000667.2:g.56875100G>A	GRCh38
NC_000005.9:g.56170927G>A , CM000667.1:g.56170927G>A	GRCh37
NC_000005.8:g.56206684G>A	NCBI36
NG_031884.1:g.65028G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1755G>A MANE Select	ENSP00000382423.3:p.Arg585=
ENST00000399503.3:c.1755G>A	ENSP00000382423.3:p.Arg585=
NM_005921.1:c.1755G>A	NP_005912.1:p.Arg585=
XM_005248519.3:c.1377G>A	XP_005248576.2:p.Arg459=
XM_011543406.1:c.1500G>A	XP_011541708.1:p.Arg500=
XM_011543407.1:c.1686+2095G>A	XP_011541709.1:n.1686+2095G>A
XM_011543408.1:c.1755G>A	XP_011541710.1:p.Arg585=
XM_017009484.1:c.1344G>A	XP_016864973.1:p.Arg448=
XM_017009485.1:c.1266G>A	XP_016864974.1:p.Arg422=
XR_001742068.2:n.1786G>A
NM_005921.2:c.1755G>A MANE Select	NP_005912.1:p.Arg585=