Canonical Allele Identifier: CA403383281

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095408G>T , CM000681.2:g.4095408G>T	GRCh38
NC_000019.9:g.4095406G>T , CM000681.1:g.4095406G>T	GRCh37
NC_000019.8:g.4046406G>T	NCBI36
NG_007996.1:g.33721C>A , LRG_750:g.33721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1465C>A
ENST00000688002.1:n.3177C>A
ENST00000688751.1:n.162C>A
ENST00000689792.1:n.930C>A
ENST00000262948.10:c.1026C>A MANE Select	ENSP00000262948.4:p.Phe342Leu
ENST00000262948.9:c.1026C>A	ENSP00000262948.3:p.Phe342Leu
ENST00000394867.8:c.735C>A	ENSP00000378336.1:p.Phe245Leu
ENST00000595715.1:n.841C>A
ENST00000597263.5:n.211C>A
ENST00000599021.1:c.136C>A
ENST00000600584.5:n.1586C>A
ENST00000601786.5:n.1327C>A
NM_030662.3:c.1026C>A , LRG_750t1:c.1026C>A	NP_109587.1:p.Phe342Leu
XM_006722799.2:c.747C>A	XP_006722862.1:p.Phe249Leu
XM_011528133.1:c.456C>A	XP_011526435.1:p.Phe152Leu
XM_017026989.1:c.1026C>A	XP_016882478.1:p.Phe342Leu
XM_017026990.1:c.747C>A	XP_016882479.1:p.Phe249Leu
NM_030662.4:c.1026C>A MANE Select	NP_109587.1:p.Phe342Leu