Canonical Allele Identifier: CA359787726

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945933
• MyVariant Identifiers: chr5:g.56178158C>A (hg19) ; chr5:g.56882331C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882331C>A , CM000667.2:g.56882331C>A	GRCh38
NC_000005.9:g.56178158C>A , CM000667.1:g.56178158C>A	GRCh37
NC_000005.8:g.56213915C>A	NCBI36
NG_031884.1:g.72259C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3131C>A MANE Select	ENSP00000382423.3:p.Pro1044Gln
ENST00000399503.3:c.3131C>A	ENSP00000382423.3:p.Pro1044Gln
NM_005921.1:c.3131C>A	NP_005912.1:p.Pro1044Gln
XM_005248519.3:c.2753C>A	XP_005248576.2:p.Pro918Gln
XM_011543406.1:c.2876C>A	XP_011541708.1:p.Pro959Gln
XM_011543407.1:c.2852C>A	XP_011541709.1:p.Pro951Gln
XM_011543408.1:c.3131C>A	XP_011541710.1:p.Pro1044Gln
XM_017009484.1:c.2720C>A	XP_016864973.1:p.Pro907Gln
XM_017009485.1:c.2642C>A	XP_016864974.1:p.Pro881Gln
XR_001742068.2:n.3162C>A
NM_005921.2:c.3131C>A MANE Select	NP_005912.1:p.Pro1044Gln