Canonical Allele Identifier: CA2319219673

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090501G= , CM000681.2:g.4090501G=	GRCh38
NC_000019.9:g.4090499G= , CM000681.1:g.4090499G=	GRCh37
NC_000019.8:g.4041499G=	NCBI36
NG_007996.1:g.38628C= , LRG_750:g.38628C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1739C=
ENST00000688002.1:n.3451C=
ENST00000688751.1:n.436C=
ENST00000689792.1:n.1204C=
ENST00000262948.10:c.*97C= MANE Select	ENSP00000262948.4:n.*97C=
ENST00000262948.9:c.*97C=	ENSP00000262948.3:n.*97C=
ENST00000394867.8:c.*97C=	ENSP00000378336.1:n.*97C=
ENST00000597263.5:n.485C=
ENST00000600584.5:n.2749C=
ENST00000601786.5:n.1601C=
NM_030662.3:c.*97C= , LRG_750t1:c.*97C=	NP_109587.1:n.*97C=
XM_006722799.2:c.*97C=	XP_006722862.1:n.*97C=
XM_011528133.1:c.*97C=	XP_011526435.1:n.*97C=
NM_030662.4:c.*97C= MANE Select	NP_109587.1:n.*97C=