Canonical Allele Identifier: CA304449840

Gene: MAP2K2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4101025G>A , CM000681.2:g.4101025G>A	GRCh38
NC_000019.9:g.4101023G>A , CM000681.1:g.4101023G>A	GRCh37
NC_000019.8:g.4052023G>A	NCBI36
NG_007996.1:g.28104C>T , LRG_750:g.28104C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1138C>T
ENST00000687128.1:n.1138C>T
ENST00000689792.1:n.639C>T
ENST00000262948.10:c.699C>T MANE Select	ENSP00000262948.4:p.Tyr233=
ENST00000262948.9:c.699C>T	ENSP00000262948.3:p.Tyr233=
ENST00000394867.8:c.408C>T	ENSP00000378336.1:p.Tyr136=
ENST00000593364.5:n.646C>T
ENST00000597008.5:n.300C>T
ENST00000597263.5:n.163C>T
ENST00000599021.1:c.23C>T
ENST00000601786.5:n.1000C>T
ENST00000602167.5:n.419C>T
NM_030662.3:c.699C>T , LRG_750t1:c.699C>T	NP_109587.1:p.Tyr233=
XM_006722799.2:c.699C>T	XP_006722862.1:p.Tyr233=
XM_011528133.1:c.129C>T	XP_011526435.1:p.Tyr43=
XM_017026989.1:c.699C>T	XP_016882478.1:p.Tyr233=
XM_017026990.1:c.699C>T	XP_016882479.1:p.Tyr233=
XM_017026991.1:c.699C>T	XP_016882480.1:p.Tyr233=
NM_030662.4:c.699C>T MANE Select	NP_109587.1:p.Tyr233=