Canonical Allele Identifier: CA2184100033

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66485086C= , CM000677.2:g.66485086C=	GRCh38
NC_000015.9:g.66777424C= , CM000677.1:g.66777424C=	GRCh37
NC_000015.8:g.64564478C=	NCBI36
NG_008305.1:g.103214C= , LRG_725:g.103214C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.628-2142C=	ENSP00000508681.1:n.628-2142C=
ENST00000685172.1:c.790C=	ENSP00000509604.1:p.Pro264=
ENST00000685763.1:c.643C=	ENSP00000509016.1:p.Pro215=
ENST00000686347.1:c.569-2142C=	ENSP00000509027.1:n.569-2142C=
ENST00000687191.1:n.1148C=
ENST00000687481.1:n.205C=
ENST00000689951.1:c.841C=	ENSP00000509308.1:p.Pro281=
ENST00000691077.1:c.*27C=	ENSP00000509843.1:n.*27C=
ENST00000691576.1:c.661C=	ENSP00000510066.1:p.Pro221=
ENST00000691937.1:c.790C=	ENSP00000508768.1:p.Pro264=
ENST00000692487.1:c.*27C=	ENSP00000509534.1:n.*27C=
ENST00000692683.1:c.724C=	ENSP00000508437.1:p.Pro242=
ENST00000693150.1:c.646C=	ENSP00000510309.1:p.Pro216=
ENST00000307102.10:c.790C= MANE Select	ENSP00000302486.5:p.Pro264=
ENST00000307102.9:c.790C=	ENSP00000302486.4:p.Pro264=
ENST00000566326.1:c.262C=	ENSP00000456438.1:p.Pro88=
NM_002755.3:c.790C= , LRG_725t1:c.790C=	NP_002746.1:p.Pro264=
XM_011521783.1:c.724C=	XP_011520085.1:p.Pro242=
XM_011521783.3:c.724C=	XP_011520085.1:p.Pro242=
XM_017022411.2:c.712C=	XP_016877900.1:p.Pro238=
XM_017022412.1:c.646C=	XP_016877901.1:p.Pro216=
XM_017022413.1:c.262C=	XP_016877902.1:p.Pro88=
NM_002755.4:c.790C= MANE Select	NP_002746.1:p.Pro264=