Canonical Allele Identifier: CA359786138

Gene: MAP3K1

Linked Data

• dbSNP Id: rs773937637
• MyVariant Identifiers: chr5:g.56177624C>T (hg19) ; chr5:g.56881797C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881797C>T , CM000667.2:g.56881797C>T	GRCh38
NC_000005.9:g.56177624C>T , CM000667.1:g.56177624C>T	GRCh37
NC_000005.8:g.56213381C>T	NCBI36
NG_031884.1:g.71725C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2597C>T MANE Select	ENSP00000382423.3:p.Ala866Val
ENST00000399503.3:c.2597C>T	ENSP00000382423.3:p.Ala866Val
NM_005921.1:c.2597C>T	NP_005912.1:p.Ala866Val
XM_005248519.3:c.2219C>T	XP_005248576.2:p.Ala740Val
XM_011543406.1:c.2342C>T	XP_011541708.1:p.Ala781Val
XM_011543407.1:c.2318C>T	XP_011541709.1:p.Ala773Val
XM_011543408.1:c.2597C>T	XP_011541710.1:p.Ala866Val
XM_017009484.1:c.2186C>T	XP_016864973.1:p.Ala729Val
XM_017009485.1:c.2108C>T	XP_016864974.1:p.Ala703Val
XR_001742068.2:n.2628C>T
NM_005921.2:c.2597C>T MANE Select	NP_005912.1:p.Ala866Val