Canonical Allele Identifier: CA2319222255

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095429G= , CM000681.2:g.4095429G=	GRCh38
NC_000019.9:g.4095427G= , CM000681.1:g.4095427G=	GRCh37
NC_000019.8:g.4046427G=	NCBI36
NG_007996.1:g.33700C= , LRG_750:g.33700C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1444C=
ENST00000688002.1:n.3156C=
ENST00000688751.1:n.141C=
ENST00000689792.1:n.909C=
ENST00000262948.10:c.1005C= MANE Select	ENSP00000262948.4:p.Asn335=
ENST00000262948.9:c.1005C=	ENSP00000262948.3:p.Asn335=
ENST00000394867.8:c.714C=	ENSP00000378336.1:p.Asn238=
ENST00000595715.1:n.820C=
ENST00000597263.5:n.190C=
ENST00000599021.1:c.115C=
ENST00000600584.5:n.1565C=
ENST00000601786.5:n.1306C=
NM_030662.3:c.1005C= , LRG_750t1:c.1005C=	NP_109587.1:p.Asn335=
XM_006722799.2:c.726C=	XP_006722862.1:p.Asn242=
XM_011528133.1:c.435C=	XP_011526435.1:p.Asn145=
XM_017026989.1:c.1005C=	XP_016882478.1:p.Asn335=
XM_017026990.1:c.726C=	XP_016882479.1:p.Asn242=
NM_030662.4:c.1005C= MANE Select	NP_109587.1:p.Asn335=