Canonical Allele Identifier: CA359780684

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56170932T>G (hg19) ; chr5:g.56875105T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875105T>G , CM000667.2:g.56875105T>G	GRCh38
NC_000005.9:g.56170932T>G , CM000667.1:g.56170932T>G	GRCh37
NC_000005.8:g.56206689T>G	NCBI36
NG_031884.1:g.65033T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1760T>G MANE Select	ENSP00000382423.3:p.Leu587Arg
ENST00000399503.3:c.1760T>G	ENSP00000382423.3:p.Leu587Arg
NM_005921.1:c.1760T>G	NP_005912.1:p.Leu587Arg
XM_005248519.3:c.1382T>G	XP_005248576.2:p.Leu461Arg
XM_011543406.1:c.1505T>G	XP_011541708.1:p.Leu502Arg
XM_011543407.1:c.1686+2100T>G	XP_011541709.1:n.1686+2100T>G
XM_011543408.1:c.1760T>G	XP_011541710.1:p.Leu587Arg
XM_017009484.1:c.1349T>G	XP_016864973.1:p.Leu450Arg
XM_017009485.1:c.1271T>G	XP_016864974.1:p.Leu424Arg
XR_001742068.2:n.1791T>G
NM_005921.2:c.1760T>G MANE Select	NP_005912.1:p.Leu587Arg