Canonical Allele Identifier: CA2184099980

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66484999C= , CM000677.2:g.66484999C=	GRCh38
NC_000015.9:g.66777337C= , CM000677.1:g.66777337C=	GRCh37
NC_000015.8:g.64564391C=	NCBI36
NG_008305.1:g.103127C= , LRG_725:g.103127C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.628-2229C=	ENSP00000508681.1:n.628-2229C=
ENST00000685172.1:c.703C=	ENSP00000509604.1:p.Leu235=
ENST00000685763.1:c.556C=	ENSP00000509016.1:p.Leu186=
ENST00000686347.1:c.569-2229C=	ENSP00000509027.1:n.569-2229C=
ENST00000687191.1:n.1061C=
ENST00000687481.1:n.118C=
ENST00000689951.1:c.754C=	ENSP00000509308.1:p.Leu252=
ENST00000691077.1:c.699C=	ENSP00000509843.1:p.Asp233=
ENST00000691576.1:c.574C=	ENSP00000510066.1:p.Leu192=
ENST00000691937.1:c.703C=	ENSP00000508768.1:p.Leu235=
ENST00000692487.1:c.699C=	ENSP00000509534.1:p.Asp233=
ENST00000692683.1:c.637C=	ENSP00000508437.1:p.Leu213=
ENST00000693150.1:c.559C=	ENSP00000510309.1:p.Leu187=
ENST00000307102.10:c.703C= MANE Select	ENSP00000302486.5:p.Leu235=
ENST00000307102.9:c.703C=	ENSP00000302486.4:p.Leu235=
ENST00000566326.1:c.175C=	ENSP00000456438.1:p.Leu59=
NM_002755.3:c.703C= , LRG_725t1:c.703C=	NP_002746.1:p.Leu235=
XM_011521783.1:c.637C=	XP_011520085.1:p.Leu213=
XM_011521783.3:c.637C=	XP_011520085.1:p.Leu213=
XM_017022411.2:c.625C=	XP_016877900.1:p.Leu209=
XM_017022412.1:c.559C=	XP_016877901.1:p.Leu187=
XM_017022413.1:c.175C=	XP_016877902.1:p.Leu59=
NM_002755.4:c.703C= MANE Select	NP_002746.1:p.Leu235=