Canonical Allele Identifier: CA359787008

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177920C>G (hg19) ; chr5:g.56882093C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882093C>G , CM000667.2:g.56882093C>G	GRCh38
NC_000005.9:g.56177920C>G , CM000667.1:g.56177920C>G	GRCh37
NC_000005.8:g.56213677C>G	NCBI36
NG_031884.1:g.72021C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2893C>G MANE Select	ENSP00000382423.3:p.Gln965Glu
ENST00000399503.3:c.2893C>G	ENSP00000382423.3:p.Gln965Glu
NM_005921.1:c.2893C>G	NP_005912.1:p.Gln965Glu
XM_005248519.3:c.2515C>G	XP_005248576.2:p.Gln839Glu
XM_011543406.1:c.2638C>G	XP_011541708.1:p.Gln880Glu
XM_011543407.1:c.2614C>G	XP_011541709.1:p.Gln872Glu
XM_011543408.1:c.2893C>G	XP_011541710.1:p.Gln965Glu
XM_017009484.1:c.2482C>G	XP_016864973.1:p.Gln828Glu
XM_017009485.1:c.2404C>G	XP_016864974.1:p.Gln802Glu
XR_001742068.2:n.2924C>G
NM_005921.2:c.2893C>G MANE Select	NP_005912.1:p.Gln965Glu