Canonical Allele Identifier: CA359786651

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1748226177
• MyVariant Identifiers: chr5:g.56177824A>C (hg19) ; chr5:g.56881997A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881997A>C , CM000667.2:g.56881997A>C	GRCh38
NC_000005.9:g.56177824A>C , CM000667.1:g.56177824A>C	GRCh37
NC_000005.8:g.56213581A>C	NCBI36
NG_031884.1:g.71925A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2797A>C MANE Select	ENSP00000382423.3:p.Ser933Arg
ENST00000399503.3:c.2797A>C	ENSP00000382423.3:p.Ser933Arg
NM_005921.1:c.2797A>C	NP_005912.1:p.Ser933Arg
XM_005248519.3:c.2419A>C	XP_005248576.2:p.Ser807Arg
XM_011543406.1:c.2542A>C	XP_011541708.1:p.Ser848Arg
XM_011543407.1:c.2518A>C	XP_011541709.1:p.Ser840Arg
XM_011543408.1:c.2797A>C	XP_011541710.1:p.Ser933Arg
XM_017009484.1:c.2386A>C	XP_016864973.1:p.Ser796Arg
XM_017009485.1:c.2308A>C	XP_016864974.1:p.Ser770Arg
XR_001742068.2:n.2828A>C
NM_005921.2:c.2797A>C MANE Select	NP_005912.1:p.Ser933Arg