Canonical Allele Identifier: CA2184097451

Gene: MAP2K1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66481841A= , CM000677.2:g.66481841A=	GRCh38
NC_000015.9:g.66774179A= , CM000677.1:g.66774179A=	GRCh37
NC_000015.8:g.64561233A=	NCBI36
NG_008305.1:g.99969A= , LRG_725:g.99969A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684779.1:c.589A=	ENSP00000508681.1:p.Met197=
ENST00000685172.1:c.655A=	ENSP00000509604.1:p.Met219=
ENST00000685763.1:c.508A=	ENSP00000509016.1:p.Met170=
ENST00000686347.1:c.569-5387A=	ENSP00000509027.1:n.569-5387A=
ENST00000687191.1:n.1013A=
ENST00000689951.1:c.706A=	ENSP00000509308.1:p.Met236=
ENST00000691077.1:c.655A=	ENSP00000509843.1:p.Met219=
ENST00000691576.1:c.569-3153A=	ENSP00000510066.1:n.569-3153A=
ENST00000691937.1:c.655A=	ENSP00000508768.1:p.Met219=
ENST00000692487.1:c.655A=	ENSP00000509534.1:p.Met219=
ENST00000692683.1:c.589A=	ENSP00000508437.1:p.Met197=
ENST00000693150.1:c.511A=	ENSP00000510309.1:p.Met171=
ENST00000307102.10:c.655A= MANE Select	ENSP00000302486.5:p.Met219=
ENST00000307102.9:c.655A=	ENSP00000302486.4:p.Met219=
ENST00000566326.1:c.127A=	ENSP00000456438.1:p.Met43=
NM_002755.3:c.655A= , LRG_725t1:c.655A=	NP_002746.1:p.Met219=
XM_011521783.1:c.589A=	XP_011520085.1:p.Met197=
XM_011521783.3:c.589A=	XP_011520085.1:p.Met197=
XM_017022411.2:c.577A=	XP_016877900.1:p.Met193=
XM_017022412.1:c.511A=	XP_016877901.1:p.Met171=
XM_017022413.1:c.127A=	XP_016877902.1:p.Met43=
NM_002755.4:c.655A= MANE Select	NP_002746.1:p.Met219=