Canonical Allele Identifier: CA296148

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4097325C>T , CM000681.2:g.4097325C>T	GRCh38
NC_000019.9:g.4097323C>T , CM000681.1:g.4097323C>T	GRCh37
NC_000019.8:g.4048323C>T	NCBI36
NG_007996.1:g.31804G>A , LRG_750:g.31804G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_030662.4:c.938G>A MANE Select	NP_109587.1:p.Arg313Gln
ENST00000262948.10:c.938G>A MANE Select	ENSP00000262948.4:p.Arg313Gln
NM_030662.3:c.938G>A , LRG_750t1:c.938G>A	NP_109587.1:p.Arg313Gln
ENST00000262948.9:c.938G>A	ENSP00000262948.3:p.Arg313Gln
ENST00000394867.8:c.647G>A	ENSP00000378336.1:p.Arg216Gln
ENST00000394867.9:n.1377G>A
ENST00000595715.1:n.753G>A
ENST00000597263.5:n.170-1876G>A
ENST00000599021.1:c.48G>A
ENST00000600584.5:n.1498G>A
ENST00000601786.5:n.1239G>A
ENST00000687128.1:n.2188G>A
ENST00000688002.1:n.3089G>A
ENST00000689792.1:n.842G>A
XM_006722799.2:c.706-1876G>A	XP_006722862.1:n.706-1876G>A
XM_011528133.1:c.368G>A	XP_011526435.1:p.Arg123Gln
XM_017026989.1:c.938G>A	XP_016882478.1:p.Arg313Gln
XM_017026990.1:c.706-1876G>A	XP_016882479.1:n.706-1876G>A