Canonical Allele Identifier: CA359787540

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945097
• MyVariant Identifiers: chr5:g.56178073T>C (hg19) ; chr5:g.56882246T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882246T>C , CM000667.2:g.56882246T>C	GRCh38
NC_000005.9:g.56178073T>C , CM000667.1:g.56178073T>C	GRCh37
NC_000005.8:g.56213830T>C	NCBI36
NG_031884.1:g.72174T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3046T>C MANE Select	ENSP00000382423.3:p.Ser1016Pro
ENST00000399503.3:c.3046T>C	ENSP00000382423.3:p.Ser1016Pro
NM_005921.1:c.3046T>C	NP_005912.1:p.Ser1016Pro
XM_005248519.3:c.2668T>C	XP_005248576.2:p.Ser890Pro
XM_011543406.1:c.2791T>C	XP_011541708.1:p.Ser931Pro
XM_011543407.1:c.2767T>C	XP_011541709.1:p.Ser923Pro
XM_011543408.1:c.3046T>C	XP_011541710.1:p.Ser1016Pro
XM_017009484.1:c.2635T>C	XP_016864973.1:p.Ser879Pro
XM_017009485.1:c.2557T>C	XP_016864974.1:p.Ser853Pro
XR_001742068.2:n.3077T>C
NM_005921.2:c.3046T>C MANE Select	NP_005912.1:p.Ser1016Pro