Canonical Allele Identifier: CA2319219716

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090578C= , CM000681.2:g.4090578C=	GRCh38
NC_000019.9:g.4090576C= , CM000681.1:g.4090576C=	GRCh37
NC_000019.8:g.4041576C=	NCBI36
NG_007996.1:g.38551G= , LRG_750:g.38551G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1662G=
ENST00000688002.1:n.3374G=
ENST00000688751.1:n.359G=
ENST00000689792.1:n.1127G=
ENST00000262948.10:c.*20G= MANE Select	ENSP00000262948.4:n.*20G=
ENST00000262948.9:c.*20G=	ENSP00000262948.3:n.*20G=
ENST00000394867.8:c.*20G=	ENSP00000378336.1:n.*20G=
ENST00000597263.5:n.408G=
ENST00000600584.5:n.2672G=
ENST00000601786.5:n.1524G=
NM_030662.3:c.*20G= , LRG_750t1:c.*20G=	NP_109587.1:n.*20G=
XM_006722799.2:c.*20G=	XP_006722862.1:n.*20G=
XM_011528133.1:c.*20G=	XP_011526435.1:n.*20G=
NM_030662.4:c.*20G= MANE Select	NP_109587.1:n.*20G=