Canonical Allele Identifier: CA359786023

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111941519
• MyVariant Identifiers: chr5:g.56177570A>C (hg19) ; chr5:g.56881743A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881743A>C , CM000667.2:g.56881743A>C	GRCh38
NC_000005.9:g.56177570A>C , CM000667.1:g.56177570A>C	GRCh37
NC_000005.8:g.56213327A>C	NCBI36
NG_031884.1:g.71671A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2543A>C MANE Select	ENSP00000382423.3:p.His848Pro
ENST00000399503.3:c.2543A>C	ENSP00000382423.3:p.His848Pro
NM_005921.1:c.2543A>C	NP_005912.1:p.His848Pro
XM_005248519.3:c.2165A>C	XP_005248576.2:p.His722Pro
XM_011543406.1:c.2288A>C	XP_011541708.1:p.His763Pro
XM_011543407.1:c.2264A>C	XP_011541709.1:p.His755Pro
XM_011543408.1:c.2543A>C	XP_011541710.1:p.His848Pro
XM_017009484.1:c.2132A>C	XP_016864973.1:p.His711Pro
XM_017009485.1:c.2054A>C	XP_016864974.1:p.His685Pro
XR_001742068.2:n.2574A>C
NM_005921.2:c.2543A>C MANE Select	NP_005912.1:p.His848Pro