Canonical Allele Identifier: CA2184097442

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66481830T= , CM000677.2:g.66481830T=	GRCh38
NC_000015.9:g.66774168T= , CM000677.1:g.66774168T=	GRCh37
NC_000015.8:g.64561222T=	NCBI36
NG_008305.1:g.99958T= , LRG_725:g.99958T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.578T=	ENSP00000508681.1:p.Leu193=
ENST00000685172.1:c.644T=	ENSP00000509604.1:p.Leu215=
ENST00000685763.1:c.497T=	ENSP00000509016.1:p.Leu166=
ENST00000686347.1:c.569-5398T=	ENSP00000509027.1:n.569-5398T=
ENST00000687191.1:n.1002T=
ENST00000689951.1:c.695T=	ENSP00000509308.1:p.Leu232=
ENST00000691077.1:c.644T=	ENSP00000509843.1:p.Leu215=
ENST00000691576.1:c.569-3164T=	ENSP00000510066.1:n.569-3164T=
ENST00000691937.1:c.644T=	ENSP00000508768.1:p.Leu215=
ENST00000692487.1:c.644T=	ENSP00000509534.1:p.Leu215=
ENST00000692683.1:c.578T=	ENSP00000508437.1:p.Leu193=
ENST00000693150.1:c.500T=	ENSP00000510309.1:p.Leu167=
ENST00000307102.10:c.644T= MANE Select	ENSP00000302486.5:p.Leu215=
ENST00000307102.9:c.644T=	ENSP00000302486.4:p.Leu215=
ENST00000566326.1:c.116T=	ENSP00000456438.1:p.Leu39=
NM_002755.3:c.644T= , LRG_725t1:c.644T=	NP_002746.1:p.Leu215=
XM_011521783.1:c.578T=	XP_011520085.1:p.Leu193=
XM_011521783.3:c.578T=	XP_011520085.1:p.Leu193=
XM_017022411.2:c.566T=	XP_016877900.1:p.Leu189=
XM_017022412.1:c.500T=	XP_016877901.1:p.Leu167=
XM_017022413.1:c.116T=	XP_016877902.1:p.Leu39=
NM_002755.4:c.644T= MANE Select	NP_002746.1:p.Leu215=