Canonical Allele Identifier: CA2735392379

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2040969612

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099456A>C , CM000681.2:g.4099456A>C	GRCh38
NC_000019.9:g.4099454A>C , CM000681.1:g.4099454A>C	GRCh37
NC_000019.8:g.4050454A>C	NCBI36
NG_007996.1:g.29673T>G , LRG_750:g.29673T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-42T>G
ENST00000687128.1:n.1145-42T>G
ENST00000688002.1:n.958T>G
ENST00000689792.1:n.646-78T>G
ENST00000262948.10:c.706-42T>G MANE Select	ENSP00000262948.4:n.706-42T>G
ENST00000262948.9:c.706-42T>G	ENSP00000262948.3:n.706-42T>G
ENST00000394867.8:c.415-42T>G	ENSP00000378336.1:n.415-42T>G
ENST00000593364.5:n.653-42T>G
ENST00000595715.1:n.479T>G
ENST00000597263.5:n.169+1563T>G
ENST00000599021.1:c.29+1563T>G
ENST00000600584.5:n.1224T>G
ENST00000601786.5:n.1007-42T>G
ENST00000602167.5:n.426-42T>G
NM_030662.3:c.706-42T>G , LRG_750t1:c.706-42T>G	NP_109587.1:n.706-42T>G
XM_006722799.2:c.705+1563T>G	XP_006722862.1:n.705+1563T>G
XM_011528133.1:c.136-42T>G	XP_011526435.1:n.136-42T>G
XM_017026989.1:c.706-42T>G	XP_016882478.1:n.706-42T>G
XM_017026990.1:c.705+1563T>G	XP_016882479.1:n.705+1563T>G
XM_017026991.1:c.*274T>G	XP_016882480.1:n.*274T>G
NM_030662.4:c.706-42T>G MANE Select	NP_109587.1:n.706-42T>G