Canonical Allele Identifier: CA2319222364

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095629A= , CM000681.2:g.4095629A=	GRCh38
NC_000019.9:g.4095627A= , CM000681.1:g.4095627A=	GRCh37
NC_000019.8:g.4046627A=	NCBI36
NG_007996.1:g.33500T= , LRG_750:g.33500T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-180T=
ENST00000688002.1:n.3136-180T=
ENST00000688751.1:n.121-180T=
ENST00000689792.1:n.889-180T=
ENST00000262948.10:c.985-180T= MANE Select	ENSP00000262948.4:n.985-180T=
ENST00000262948.9:c.985-180T=	ENSP00000262948.3:n.985-180T=
ENST00000394867.8:c.694-180T=	ENSP00000378336.1:n.694-180T=
ENST00000595715.1:n.800-180T=
ENST00000597263.5:n.170-180T=
ENST00000599021.1:c.95-180T=
ENST00000600584.5:n.1545-180T=
ENST00000601786.5:n.1286-180T=
NM_030662.3:c.985-180T= , LRG_750t1:c.985-180T=	NP_109587.1:n.985-180T=
XM_006722799.2:c.706-180T=	XP_006722862.1:n.706-180T=
XM_011528133.1:c.415-180T=	XP_011526435.1:n.415-180T=
XM_017026989.1:c.985-180T=	XP_016882478.1:n.985-180T=
XM_017026990.1:c.706-180T=	XP_016882479.1:n.706-180T=
NM_030662.4:c.985-180T= MANE Select	NP_109587.1:n.985-180T=