Canonical Allele Identifier: CA2319234280

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117430T= , CM000681.2:g.4117430T=	GRCh38
NC_000019.9:g.4117428T= , CM000681.1:g.4117428T=	GRCh37
NC_000019.8:g.4068428T=	NCBI36
NG_007996.1:g.11699A= , LRG_750:g.11699A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.731A=
ENST00000687128.1:n.731A=
ENST00000262948.10:c.292A= MANE Select	ENSP00000262948.4:p.Met98=
ENST00000262948.9:c.292A=	ENSP00000262948.3:p.Met98=
ENST00000394867.8:c.1A=	ENSP00000378336.1:p.Met1=
ENST00000599345.1:n.489A=
NM_030662.3:c.292A= , LRG_750t1:c.292A=	NP_109587.1:p.Met98=
XM_006722799.2:c.292A=	XP_006722862.1:p.Met98=
XM_017026989.1:c.292A=	XP_016882478.1:p.Met98=
XM_017026990.1:c.292A=	XP_016882479.1:p.Met98=
XM_017026991.1:c.292A=	XP_016882480.1:p.Met98=
NM_030662.4:c.292A= MANE Select	NP_109587.1:p.Met98=