Canonical Allele Identifier: CA2813356260

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094194C>T , CM000681.2:g.4094194C>T	GRCh38
NC_000019.9:g.4094192C>T , CM000681.1:g.4094192C>T	GRCh37
NC_000019.8:g.4045192C>T	NCBI36
NG_007996.1:g.34935G>A , LRG_750:g.34935G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1531+259G>A
ENST00000688002.1:n.3243+259G>A
ENST00000688751.1:n.228+259G>A
ENST00000689792.1:n.996+259G>A
ENST00000262948.10:c.1092+259G>A MANE Select	ENSP00000262948.4:n.1092+259G>A
ENST00000262948.9:c.1092+259G>A	ENSP00000262948.3:n.1092+259G>A
ENST00000394867.8:c.801+259G>A	ENSP00000378336.1:n.801+259G>A
ENST00000597263.5:n.277+259G>A
ENST00000599021.1:c.202+259G>A
ENST00000600584.5:n.2541+259G>A
ENST00000601786.5:n.1393+259G>A
NM_030662.3:c.1092+259G>A , LRG_750t1:c.1092+259G>A	NP_109587.1:n.1092+259G>A
XM_006722799.2:c.813+259G>A	XP_006722862.1:n.813+259G>A
XM_011528133.1:c.522+259G>A	XP_011526435.1:n.522+259G>A
NM_030662.4:c.1092+259G>A MANE Select	NP_109587.1:n.1092+259G>A