Canonical Allele Identifier: CA2319221727

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094539G= , CM000681.2:g.4094539G=	GRCh38
NC_000019.9:g.4094537G= , CM000681.1:g.4094537G=	GRCh37
NC_000019.8:g.4045537G=	NCBI36
NG_007996.1:g.34590C= , LRG_750:g.34590C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-41C=
ENST00000688002.1:n.3198-41C=
ENST00000688751.1:n.183-41C=
ENST00000689792.1:n.951-41C=
ENST00000262948.10:c.1047-41C= MANE Select	ENSP00000262948.4:n.1047-41C=
ENST00000262948.9:c.1047-41C=	ENSP00000262948.3:n.1047-41C=
ENST00000394867.8:c.756-41C=	ENSP00000378336.1:n.756-41C=
ENST00000597263.5:n.232-41C=
ENST00000599021.1:c.157-41C=
ENST00000600584.5:n.2455C=
ENST00000601786.5:n.1348-41C=
NM_030662.3:c.1047-41C= , LRG_750t1:c.1047-41C=	NP_109587.1:n.1047-41C=
XM_006722799.2:c.768-41C=	XP_006722862.1:n.768-41C=
XM_011528133.1:c.477-41C=	XP_011526435.1:n.477-41C=
XM_017026989.1:c.*15C=	XP_016882478.1:n.*15C=
XM_017026990.1:c.*15C=	XP_016882479.1:n.*15C=
NM_030662.4:c.1047-41C= MANE Select	NP_109587.1:n.1047-41C=