Canonical Allele Identifier: CA2184097307

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66481637G= , CM000677.2:g.66481637G=	GRCh38
NC_000015.9:g.66773975G= , CM000677.1:g.66773975G=	GRCh37
NC_000015.8:g.64561029G=	NCBI36
NG_008305.1:g.99765G= , LRG_725:g.99765G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.503-118G=	ENSP00000508681.1:n.503-118G=
ENST00000685172.1:c.569-118G=	ENSP00000509604.1:n.569-118G=
ENST00000685763.1:c.422-118G=	ENSP00000509016.1:n.422-118G=
ENST00000686347.1:c.569-5591G=	ENSP00000509027.1:n.569-5591G=
ENST00000687191.1:n.927-118G=
ENST00000689951.1:c.620-118G=	ENSP00000509308.1:n.620-118G=
ENST00000691077.1:c.569-118G=	ENSP00000509843.1:n.569-118G=
ENST00000691576.1:c.569-3357G=	ENSP00000510066.1:n.569-3357G=
ENST00000691937.1:c.569-118G=	ENSP00000508768.1:n.569-118G=
ENST00000692487.1:c.569-118G=	ENSP00000509534.1:n.569-118G=
ENST00000692683.1:c.503-118G=	ENSP00000508437.1:n.503-118G=
ENST00000693150.1:c.425-118G=	ENSP00000510309.1:n.425-118G=
ENST00000307102.10:c.569-118G= MANE Select	ENSP00000302486.5:n.569-118G=
ENST00000307102.9:c.569-118G=	ENSP00000302486.4:n.569-118G=
ENST00000566326.1:c.41-118G=	ENSP00000456438.1:n.41-118G=
NM_002755.3:c.569-118G= , LRG_725t1:c.569-118G=	NP_002746.1:n.569-118G=
XM_011521783.1:c.503-118G=	XP_011520085.1:n.503-118G=
XM_011521783.3:c.503-118G=	XP_011520085.1:n.503-118G=
XM_017022411.2:c.491-118G=	XP_016877900.1:n.491-118G=
XM_017022412.1:c.425-118G=	XP_016877901.1:n.425-118G=
XM_017022413.1:c.41-118G=	XP_016877902.1:n.41-118G=
NM_002755.4:c.569-118G= MANE Select	NP_002746.1:n.569-118G=