Canonical Allele Identifier: CA359785955

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177539T>G (hg19) ; chr5:g.56881712T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881712T>G , CM000667.2:g.56881712T>G	GRCh38
NC_000005.9:g.56177539T>G , CM000667.1:g.56177539T>G	GRCh37
NC_000005.8:g.56213296T>G	NCBI36
NG_031884.1:g.71640T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2512T>G MANE Select	ENSP00000382423.3:p.Leu838Val
ENST00000399503.3:c.2512T>G	ENSP00000382423.3:p.Leu838Val
NM_005921.1:c.2512T>G	NP_005912.1:p.Leu838Val
XM_005248519.3:c.2134T>G	XP_005248576.2:p.Leu712Val
XM_011543406.1:c.2257T>G	XP_011541708.1:p.Leu753Val
XM_011543407.1:c.2233T>G	XP_011541709.1:p.Leu745Val
XM_011543408.1:c.2512T>G	XP_011541710.1:p.Leu838Val
XM_017009484.1:c.2101T>G	XP_016864973.1:p.Leu701Val
XM_017009485.1:c.2023T>G	XP_016864974.1:p.Leu675Val
XR_001742068.2:n.2543T>G
NM_005921.2:c.2512T>G MANE Select	NP_005912.1:p.Leu838Val