Canonical Allele Identifier: CA359787513

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178061T>G (hg19) ; chr5:g.56882234T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882234T>G , CM000667.2:g.56882234T>G	GRCh38
NC_000005.9:g.56178061T>G , CM000667.1:g.56178061T>G	GRCh37
NC_000005.8:g.56213818T>G	NCBI36
NG_031884.1:g.72162T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3034T>G MANE Select	ENSP00000382423.3:p.Cys1012Gly
ENST00000399503.3:c.3034T>G	ENSP00000382423.3:p.Cys1012Gly
NM_005921.1:c.3034T>G	NP_005912.1:p.Cys1012Gly
XM_005248519.3:c.2656T>G	XP_005248576.2:p.Cys886Gly
XM_011543406.1:c.2779T>G	XP_011541708.1:p.Cys927Gly
XM_011543407.1:c.2755T>G	XP_011541709.1:p.Cys919Gly
XM_011543408.1:c.3034T>G	XP_011541710.1:p.Cys1012Gly
XM_017009484.1:c.2623T>G	XP_016864973.1:p.Cys875Gly
XM_017009485.1:c.2545T>G	XP_016864974.1:p.Cys849Gly
XR_001742068.2:n.3065T>G
NM_005921.2:c.3034T>G MANE Select	NP_005912.1:p.Cys1012Gly