Canonical Allele Identifier: CA444391754

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155700A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859873A>G , CM000667.2:g.56859873A>G	GRCh38
NC_000005.9:g.56155700A>G , CM000667.1:g.56155700A>G	GRCh37
NC_000005.8:g.56191457A>G	NCBI36
NG_031884.1:g.49801A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.792A>G MANE Select	ENSP00000382423.3:p.Ser264=
ENST00000399503.3:c.792A>G	ENSP00000382423.3:p.Ser264=
NM_005921.1:c.792A>G	NP_005912.1:p.Ser264=
XM_005248519.3:c.414A>G	XP_005248576.2:p.Ser138=
XM_011543406.1:c.537A>G	XP_011541708.1:p.Ser179=
XM_011543407.1:c.792A>G	XP_011541709.1:p.Ser264=
XM_011543408.1:c.792A>G	XP_011541710.1:p.Ser264=
XM_017009484.1:c.381A>G	XP_016864973.1:p.Ser127=
XM_017009485.1:c.303A>G	XP_016864974.1:p.Ser101=
XR_001742068.2:n.823A>G
NM_005921.2:c.792A>G MANE Select	NP_005912.1:p.Ser264=