Canonical Allele Identifier: CA359786893

Gene: MAP3K1

Linked Data

• COSMIC: COSM5026315
• MyVariant Identifiers: chr5:g.56177896C>T (hg19) ; chr5:g.56882069C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882069C>T , CM000667.2:g.56882069C>T	GRCh38
NC_000005.9:g.56177896C>T , CM000667.1:g.56177896C>T	GRCh37
NC_000005.8:g.56213653C>T	NCBI36
NG_031884.1:g.71997C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2869C>T MANE Select	ENSP00000382423.3:p.Gln957Ter
ENST00000399503.3:c.2869C>T	ENSP00000382423.3:p.Gln957Ter
NM_005921.1:c.2869C>T	NP_005912.1:p.Gln957Ter
XM_005248519.3:c.2491C>T	XP_005248576.2:p.Gln831Ter
XM_011543406.1:c.2614C>T	XP_011541708.1:p.Gln872Ter
XM_011543407.1:c.2590C>T	XP_011541709.1:p.Gln864Ter
XM_011543408.1:c.2869C>T	XP_011541710.1:p.Gln957Ter
XM_017009484.1:c.2458C>T	XP_016864973.1:p.Gln820Ter
XM_017009485.1:c.2380C>T	XP_016864974.1:p.Gln794Ter
XR_001742068.2:n.2900C>T
NM_005921.2:c.2869C>T MANE Select	NP_005912.1:p.Gln957Ter