Canonical Allele Identifier: CA2184097283

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66481580T= , CM000677.2:g.66481580T=	GRCh38
NC_000015.9:g.66773918T= , CM000677.1:g.66773918T=	GRCh37
NC_000015.8:g.64560972T=	NCBI36
NG_008305.1:g.99708T= , LRG_725:g.99708T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.503-175T=	ENSP00000508681.1:n.503-175T=
ENST00000685172.1:c.569-175T=	ENSP00000509604.1:n.569-175T=
ENST00000685763.1:c.422-175T=	ENSP00000509016.1:n.422-175T=
ENST00000686347.1:c.569-5648T=	ENSP00000509027.1:n.569-5648T=
ENST00000687191.1:n.927-175T=
ENST00000689951.1:c.620-175T=	ENSP00000509308.1:n.620-175T=
ENST00000691077.1:c.569-175T=	ENSP00000509843.1:n.569-175T=
ENST00000691576.1:c.569-3414T=	ENSP00000510066.1:n.569-3414T=
ENST00000691937.1:c.569-175T=	ENSP00000508768.1:n.569-175T=
ENST00000692487.1:c.569-175T=	ENSP00000509534.1:n.569-175T=
ENST00000692683.1:c.503-175T=	ENSP00000508437.1:n.503-175T=
ENST00000693150.1:c.425-175T=	ENSP00000510309.1:n.425-175T=
ENST00000307102.10:c.569-175T= MANE Select	ENSP00000302486.5:n.569-175T=
ENST00000307102.9:c.569-175T=	ENSP00000302486.4:n.569-175T=
ENST00000566326.1:c.41-175T=	ENSP00000456438.1:n.41-175T=
NM_002755.3:c.569-175T= , LRG_725t1:c.569-175T=	NP_002746.1:n.569-175T=
XM_011521783.1:c.503-175T=	XP_011520085.1:n.503-175T=
XM_011521783.3:c.503-175T=	XP_011520085.1:n.503-175T=
XM_017022411.2:c.491-175T=	XP_016877900.1:n.491-175T=
XM_017022412.1:c.425-175T=	XP_016877901.1:n.425-175T=
XM_017022413.1:c.41-175T=	XP_016877902.1:n.41-175T=
NM_002755.4:c.569-175T= MANE Select	NP_002746.1:n.569-175T=