Canonical Allele Identifier: CA2584878580

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099496-CCGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099498_4099500del , CM000681.2:g.4099498_4099500del	GRCh38
NC_000019.9:g.4099496_4099498del , CM000681.1:g.4099496_4099498del	GRCh37
NC_000019.8:g.4050496_4050498del	NCBI36
NG_007996.1:g.29630_29632del , LRG_750:g.29630_29632del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-85_1145-83del
ENST00000687128.1:n.1145-85_1145-83del
ENST00000688002.1:n.915_917del
ENST00000689792.1:n.646-121_646-119del
ENST00000262948.10:c.706-85_706-83del MANE Select	ENSP00000262948.4:n.706-85_706-83del
ENST00000262948.9:c.706-85_706-83del	ENSP00000262948.3:n.706-85_706-83del
ENST00000394867.8:c.415-85_415-83del	ENSP00000378336.1:n.415-85_415-83del
ENST00000593364.5:n.653-85_653-83del
ENST00000595715.1:n.436_438del
ENST00000597263.5:n.169+1520_169+1522del
ENST00000599021.1:c.29+1520_29+1522del
ENST00000600584.5:n.1181_1183del
ENST00000601786.5:n.1007-85_1007-83del
ENST00000602167.5:n.426-85_426-83del
NM_030662.3:c.706-85_706-83del , LRG_750t1:c.706-85_706-83del	NP_109587.1:n.706-85_706-83del
XM_006722799.2:c.705+1520_705+1522del	XP_006722862.1:n.705+1520_705+1522del
XM_011528133.1:c.136-85_136-83del	XP_011526435.1:n.136-85_136-83del
XM_017026989.1:c.706-85_706-83del	XP_016882478.1:n.706-85_706-83del
XM_017026990.1:c.705+1520_705+1522del	XP_016882479.1:n.705+1520_705+1522del
XM_017026991.1:c.*231_*233del	XP_016882480.1:n.*231_*233del
NM_030662.4:c.706-85_706-83del MANE Select	NP_109587.1:n.706-85_706-83del