Canonical Allele Identifier: CA2584878554

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099469-CCCGGGAGGCTTGCCCCGTTACAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099472_4099494del , CM000681.2:g.4099472_4099494del	GRCh38
NC_000019.9:g.4099470_4099492del , CM000681.1:g.4099470_4099492del	GRCh37
NC_000019.8:g.4050470_4050492del	NCBI36
NG_007996.1:g.29637_29659del , LRG_750:g.29637_29659del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-78_1145-56del
ENST00000687128.1:n.1145-78_1145-56del
ENST00000688002.1:n.922_944del
ENST00000689792.1:n.646-114_646-92del
ENST00000262948.10:c.706-78_706-56del MANE Select	ENSP00000262948.4:n.706-78_706-56del
ENST00000262948.9:c.706-78_706-56del	ENSP00000262948.3:n.706-78_706-56del
ENST00000394867.8:c.415-78_415-56del	ENSP00000378336.1:n.415-78_415-56del
ENST00000593364.5:n.653-78_653-56del
ENST00000595715.1:n.443_465del
ENST00000597263.5:n.169+1527_169+1549del
ENST00000599021.1:c.29+1527_29+1549del
ENST00000600584.5:n.1188_1210del
ENST00000601786.5:n.1007-78_1007-56del
ENST00000602167.5:n.426-78_426-56del
NM_030662.3:c.706-78_706-56del , LRG_750t1:c.706-78_706-56del	NP_109587.1:n.706-78_706-56del
XM_006722799.2:c.705+1527_705+1549del	XP_006722862.1:n.705+1527_705+1549del
XM_011528133.1:c.136-78_136-56del	XP_011526435.1:n.136-78_136-56del
XM_017026989.1:c.706-78_706-56del	XP_016882478.1:n.706-78_706-56del
XM_017026990.1:c.705+1527_705+1549del	XP_016882479.1:n.705+1527_705+1549del
XM_017026991.1:c.*238_*260del	XP_016882480.1:n.*238_*260del
NM_030662.4:c.706-78_706-56del MANE Select	NP_109587.1:n.706-78_706-56del