Canonical Allele Identifier: CA359786167

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177638T>G (hg19) ; chr5:g.56881811T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881811T>G , CM000667.2:g.56881811T>G	GRCh38
NC_000005.9:g.56177638T>G , CM000667.1:g.56177638T>G	GRCh37
NC_000005.8:g.56213395T>G	NCBI36
NG_031884.1:g.71739T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2611T>G MANE Select	ENSP00000382423.3:p.Leu871Val
ENST00000399503.3:c.2611T>G	ENSP00000382423.3:p.Leu871Val
NM_005921.1:c.2611T>G	NP_005912.1:p.Leu871Val
XM_005248519.3:c.2233T>G	XP_005248576.2:p.Leu745Val
XM_011543406.1:c.2356T>G	XP_011541708.1:p.Leu786Val
XM_011543407.1:c.2332T>G	XP_011541709.1:p.Leu778Val
XM_011543408.1:c.2611T>G	XP_011541710.1:p.Leu871Val
XM_017009484.1:c.2200T>G	XP_016864973.1:p.Leu734Val
XM_017009485.1:c.2122T>G	XP_016864974.1:p.Leu708Val
XR_001742068.2:n.2642T>G
NM_005921.2:c.2611T>G MANE Select	NP_005912.1:p.Leu871Val