Canonical Allele Identifier: CA2319219671

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090493G= , CM000681.2:g.4090493G=	GRCh38
NC_000019.9:g.4090491G= , CM000681.1:g.4090491G=	GRCh37
NC_000019.8:g.4041491G=	NCBI36
NG_007996.1:g.38636C= , LRG_750:g.38636C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1747C=
ENST00000688002.1:n.3459C=
ENST00000688751.1:n.444C=
ENST00000689792.1:n.1212C=
ENST00000262948.10:c.*105C= MANE Select	ENSP00000262948.4:n.*105C=
ENST00000262948.9:c.*105C=	ENSP00000262948.3:n.*105C=
ENST00000394867.8:c.*105C=	ENSP00000378336.1:n.*105C=
ENST00000597263.5:n.493C=
ENST00000600584.5:n.2757C=
ENST00000601786.5:n.1609C=
NM_030662.3:c.*105C= , LRG_750t1:c.*105C=	NP_109587.1:n.*105C=
XM_006722799.2:c.*105C=	XP_006722862.1:n.*105C=
XM_011528133.1:c.*105C=	XP_011526435.1:n.*105C=
NM_030662.4:c.*105C= MANE Select	NP_109587.1:n.*105C=