Canonical Allele Identifier: CA392930217

Gene: MAP2K1

Linked Data

• dbSNP Id: rs2140583321
• MyVariant Identifiers: chr15:g.66729090C>G (hg19) ; chr15:g.66436752C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66436752C>G , CM000677.2:g.66436752C>G	GRCh38
NC_000015.9:g.66729090C>G , CM000677.1:g.66729090C>G	GRCh37
NC_000015.8:g.64516144C>G	NCBI36
NG_008305.1:g.54880C>G , LRG_725:g.54880C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684779.1:c.232C>G	ENSP00000508681.1:p.His78Asp
ENST00000685172.1:c.298C>G	ENSP00000509604.1:p.His100Asp
ENST00000685763.1:c.291+1515C>G	ENSP00000509016.1:n.291+1515C>G
ENST00000686347.1:c.298C>G	ENSP00000509027.1:p.His100Asp
ENST00000687191.1:n.734C>G
ENST00000689951.1:c.298C>G	ENSP00000509308.1:p.His100Asp
ENST00000691077.1:c.298C>G	ENSP00000509843.1:p.His100Asp
ENST00000691576.1:c.298C>G	ENSP00000510066.1:p.His100Asp
ENST00000691937.1:c.298C>G	ENSP00000508768.1:p.His100Asp
ENST00000692487.1:c.298C>G	ENSP00000509534.1:p.His100Asp
ENST00000692683.1:c.232C>G	ENSP00000508437.1:p.His78Asp
ENST00000693150.1:c.232C>G	ENSP00000510309.1:p.His78Asp
ENST00000307102.10:c.298C>G MANE Select	ENSP00000302486.5:p.His100Asp
ENST00000307102.9:c.298C>G	ENSP00000302486.4:p.His100Asp
ENST00000425818.2:n.809C>G
NM_002755.3:c.298C>G , LRG_725t1:c.298C>G	NP_002746.1:p.His100Asp
XM_011521783.1:c.232C>G	XP_011520085.1:p.His78Asp
XM_011521783.3:c.232C>G	XP_011520085.1:p.His78Asp
XM_017022411.2:c.298C>G	XP_016877900.1:p.His100Asp
XM_017022412.1:c.232C>G	XP_016877901.1:p.His78Asp
NM_002755.4:c.298C>G MANE Select	NP_002746.1:p.His100Asp