Canonical Allele Identifier: CA359787548

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945122
• MyVariant Identifiers: chr5:g.56178077C>T (hg19) ; chr5:g.56882250C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882250C>T , CM000667.2:g.56882250C>T	GRCh38
NC_000005.9:g.56178077C>T , CM000667.1:g.56178077C>T	GRCh37
NC_000005.8:g.56213834C>T	NCBI36
NG_031884.1:g.72178C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3050C>T MANE Select	ENSP00000382423.3:p.Ala1017Val
ENST00000399503.3:c.3050C>T	ENSP00000382423.3:p.Ala1017Val
NM_005921.1:c.3050C>T	NP_005912.1:p.Ala1017Val
XM_005248519.3:c.2672C>T	XP_005248576.2:p.Ala891Val
XM_011543406.1:c.2795C>T	XP_011541708.1:p.Ala932Val
XM_011543407.1:c.2771C>T	XP_011541709.1:p.Ala924Val
XM_011543408.1:c.3050C>T	XP_011541710.1:p.Ala1017Val
XM_017009484.1:c.2639C>T	XP_016864973.1:p.Ala880Val
XM_017009485.1:c.2561C>T	XP_016864974.1:p.Ala854Val
XR_001742068.2:n.3081C>T
NM_005921.2:c.3050C>T MANE Select	NP_005912.1:p.Ala1017Val