Canonical Allele Identifier: CA359787650

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945599
• MyVariant Identifiers: chr5:g.56178125G>C (hg19) ; chr5:g.56882298G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882298G>C , CM000667.2:g.56882298G>C	GRCh38
NC_000005.9:g.56178125G>C , CM000667.1:g.56178125G>C	GRCh37
NC_000005.8:g.56213882G>C	NCBI36
NG_031884.1:g.72226G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3098G>C MANE Select	ENSP00000382423.3:p.Cys1033Ser
ENST00000399503.3:c.3098G>C	ENSP00000382423.3:p.Cys1033Ser
NM_005921.1:c.3098G>C	NP_005912.1:p.Cys1033Ser
XM_005248519.3:c.2720G>C	XP_005248576.2:p.Cys907Ser
XM_011543406.1:c.2843G>C	XP_011541708.1:p.Cys948Ser
XM_011543407.1:c.2819G>C	XP_011541709.1:p.Cys940Ser
XM_011543408.1:c.3098G>C	XP_011541710.1:p.Cys1033Ser
XM_017009484.1:c.2687G>C	XP_016864973.1:p.Cys896Ser
XM_017009485.1:c.2609G>C	XP_016864974.1:p.Cys870Ser
XR_001742068.2:n.3129G>C
NM_005921.2:c.3098G>C MANE Select	NP_005912.1:p.Cys1033Ser