Canonical Allele Identifier: CA137916

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117530G>A , CM000681.2:g.4117530G>A	GRCh38
NC_000019.9:g.4117528G>A , CM000681.1:g.4117528G>A	GRCh37
NC_000019.8:g.4068528G>A	NCBI36
NG_007996.1:g.11599C>T , LRG_750:g.11599C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.631C>T
ENST00000687128.1:n.631C>T
ENST00000262948.10:c.192C>T MANE Select	ENSP00000262948.4:p.Val64=
ENST00000262948.9:c.192C>T	ENSP00000262948.3:p.Val64=
ENST00000394867.8:c.-100C>T	ENSP00000378336.1:n.-100C>T
ENST00000599345.1:n.389C>T
NM_030662.3:c.192C>T , LRG_750t1:c.192C>T	NP_109587.1:p.Val64=
XM_006722799.2:c.192C>T	XP_006722862.1:p.Val64=
XM_017026989.1:c.192C>T	XP_016882478.1:p.Val64=
XM_017026990.1:c.192C>T	XP_016882479.1:p.Val64=
XM_017026991.1:c.192C>T	XP_016882480.1:p.Val64=
NM_030662.4:c.192C>T MANE Select	NP_109587.1:p.Val64=