Canonical Allele Identifier: CA359787626

Gene: MAP3K1

Linked Data

• COSMIC: COSM3617199
• MyVariant Identifiers: chr5:g.56178115C>T (hg19) ; chr5:g.56882288C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882288C>T , CM000667.2:g.56882288C>T	GRCh38
NC_000005.9:g.56178115C>T , CM000667.1:g.56178115C>T	GRCh37
NC_000005.8:g.56213872C>T	NCBI36
NG_031884.1:g.72216C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3088C>T MANE Select	ENSP00000382423.3:p.His1030Tyr
ENST00000399503.3:c.3088C>T	ENSP00000382423.3:p.His1030Tyr
NM_005921.1:c.3088C>T	NP_005912.1:p.His1030Tyr
XM_005248519.3:c.2710C>T	XP_005248576.2:p.His904Tyr
XM_011543406.1:c.2833C>T	XP_011541708.1:p.His945Tyr
XM_011543407.1:c.2809C>T	XP_011541709.1:p.His937Tyr
XM_011543408.1:c.3088C>T	XP_011541710.1:p.His1030Tyr
XM_017009484.1:c.2677C>T	XP_016864973.1:p.His893Tyr
XM_017009485.1:c.2599C>T	XP_016864974.1:p.His867Tyr
XR_001742068.2:n.3119C>T
NM_005921.2:c.3088C>T MANE Select	NP_005912.1:p.His1030Tyr