Canonical Allele Identifier: CA444399163

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177592T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881765T>G , CM000667.2:g.56881765T>G	GRCh38
NC_000005.9:g.56177592T>G , CM000667.1:g.56177592T>G	GRCh37
NC_000005.8:g.56213349T>G	NCBI36
NG_031884.1:g.71693T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2565T>G MANE Select	ENSP00000382423.3:p.Arg855=
ENST00000399503.3:c.2565T>G	ENSP00000382423.3:p.Arg855=
NM_005921.1:c.2565T>G	NP_005912.1:p.Arg855=
XM_005248519.3:c.2187T>G	XP_005248576.2:p.Arg729=
XM_011543406.1:c.2310T>G	XP_011541708.1:p.Arg770=
XM_011543407.1:c.2286T>G	XP_011541709.1:p.Arg762=
XM_011543408.1:c.2565T>G	XP_011541710.1:p.Arg855=
XM_017009484.1:c.2154T>G	XP_016864973.1:p.Arg718=
XM_017009485.1:c.2076T>G	XP_016864974.1:p.Arg692=
XR_001742068.2:n.2596T>G
NM_005921.2:c.2565T>G MANE Select	NP_005912.1:p.Arg855=