Canonical Allele Identifier: CA2319224231

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2040960319

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4098987dup , CM000681.2:g.4098987dup	GRCh38
NC_000019.9:g.4098985dup , CM000681.1:g.4098985dup	GRCh37
NC_000019.8:g.4049985dup	NCBI36
NG_007996.1:g.30142dup , LRG_750:g.30142dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+214dup
ENST00000687128.1:n.1572dup
ENST00000688002.1:n.1427dup
ENST00000689792.1:n.823+214dup
ENST00000262948.10:c.919+214dup MANE Select	ENSP00000262948.4:n.919+214dup
ENST00000262948.9:c.919+214dup	ENSP00000262948.3:n.919+214dup
ENST00000394867.8:c.628+214dup	ENSP00000378336.1:n.628+214dup
ENST00000595715.1:n.734+214dup
ENST00000597263.5:n.169+2032dup
ENST00000599021.1:c.30-1644dup
ENST00000600584.5:n.1479+214dup
ENST00000601786.5:n.1220+214dup
NM_030662.3:c.919+214dup , LRG_750t1:c.919+214dup	NP_109587.1:n.919+214dup
XM_006722799.2:c.705+2032dup	XP_006722862.1:n.705+2032dup
XM_011528133.1:c.349+214dup	XP_011526435.1:n.349+214dup
XM_017026989.1:c.919+214dup	XP_016882478.1:n.919+214dup
XM_017026990.1:c.705+2032dup	XP_016882479.1:n.705+2032dup
NM_030662.4:c.919+214dup MANE Select	NP_109587.1:n.919+214dup