Canonical Allele Identifier: CA504987162

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4101097C>T , CM000681.2:g.4101097C>T	GRCh38
NC_000019.9:g.4101095C>T , CM000681.1:g.4101095C>T	GRCh37
NC_000019.8:g.4052095C>T	NCBI36
NG_007996.1:g.28032G>A , LRG_750:g.28032G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_030662.4:c.627G>A MANE Select	NP_109587.1:p.Lys209=
ENST00000262948.10:c.627G>A MANE Select	ENSP00000262948.4:p.Lys209=
NM_030662.3:c.627G>A , LRG_750t1:c.627G>A	NP_109587.1:p.Lys209=
ENST00000262948.9:c.627G>A	ENSP00000262948.3:p.Lys209=
ENST00000394867.8:c.336G>A	ENSP00000378336.1:p.Lys112=
ENST00000394867.9:n.1066G>A
ENST00000593364.5:n.574G>A
ENST00000597008.5:n.228G>A
ENST00000597263.5:n.91G>A
ENST00000599345.1:n.897G>A
ENST00000601786.5:n.928G>A
ENST00000602167.5:n.347G>A
ENST00000687128.1:n.1066G>A
ENST00000689792.1:n.567G>A
XM_006722799.2:c.627G>A	XP_006722862.1:p.Lys209=
XM_011528133.1:c.57G>A	XP_011526435.1:p.Lys19=
XM_017026989.1:c.627G>A	XP_016882478.1:p.Lys209=
XM_017026990.1:c.627G>A	XP_016882479.1:p.Lys209=
XM_017026991.1:c.627G>A	XP_016882480.1:p.Lys209=