Canonical Allele Identifier: CA2584878627

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099555-T-TACCTCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099556_4099562dup , CM000681.2:g.4099556_4099562dup	GRCh38
NC_000019.9:g.4099554_4099560dup , CM000681.1:g.4099554_4099560dup	GRCh37
NC_000019.8:g.4050554_4050560dup	NCBI36
NG_007996.1:g.29567_29573dup , LRG_750:g.29567_29573dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-148_1145-142dup
ENST00000687128.1:n.1145-148_1145-142dup
ENST00000688002.1:n.852_858dup
ENST00000689792.1:n.646-184_646-178dup
ENST00000262948.10:c.706-148_706-142dup MANE Select	ENSP00000262948.4:n.706-148_706-142dup
ENST00000262948.9:c.706-148_706-142dup	ENSP00000262948.3:n.706-148_706-142dup
ENST00000394867.8:c.415-148_415-142dup	ENSP00000378336.1:n.415-148_415-142dup
ENST00000593364.5:n.653-148_653-142dup
ENST00000595715.1:n.373_379dup
ENST00000597263.5:n.169+1457_169+1463dup
ENST00000599021.1:c.29+1457_29+1463dup
ENST00000600584.5:n.1118_1124dup
ENST00000601786.5:n.1007-148_1007-142dup
ENST00000602167.5:n.426-148_426-142dup
NM_030662.3:c.706-148_706-142dup , LRG_750t1:c.706-148_706-142dup	NP_109587.1:n.706-148_706-142dup
XM_006722799.2:c.705+1457_705+1463dup	XP_006722862.1:n.705+1457_705+1463dup
XM_011528133.1:c.136-148_136-142dup	XP_011526435.1:n.136-148_136-142dup
XM_017026989.1:c.706-148_706-142dup	XP_016882478.1:n.706-148_706-142dup
XM_017026990.1:c.705+1457_705+1463dup	XP_016882479.1:n.705+1457_705+1463dup
XM_017026991.1:c.*168_*174dup	XP_016882480.1:n.*168_*174dup
NM_030662.4:c.706-148_706-142dup MANE Select	NP_109587.1:n.706-148_706-142dup