Canonical Allele Identifier: CA2584878575

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099492-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099497del , CM000681.2:g.4099497del	GRCh38
NC_000019.9:g.4099495del , CM000681.1:g.4099495del	GRCh37
NC_000019.8:g.4050495del	NCBI36
NG_007996.1:g.29636del , LRG_750:g.29636del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-79del
ENST00000687128.1:n.1145-79del
ENST00000688002.1:n.921del
ENST00000689792.1:n.646-115del
ENST00000262948.10:c.706-79del MANE Select	ENSP00000262948.4:n.706-79del
ENST00000262948.9:c.706-79del	ENSP00000262948.3:n.706-79del
ENST00000394867.8:c.415-79del	ENSP00000378336.1:n.415-79del
ENST00000593364.5:n.653-79del
ENST00000595715.1:n.442del
ENST00000597263.5:n.169+1526del
ENST00000599021.1:c.29+1526del
ENST00000600584.5:n.1187del
ENST00000601786.5:n.1007-79del
ENST00000602167.5:n.426-79del
NM_030662.3:c.706-79del , LRG_750t1:c.706-79del	NP_109587.1:n.706-79del
XM_006722799.2:c.705+1526del	XP_006722862.1:n.705+1526del
XM_011528133.1:c.136-79del	XP_011526435.1:n.136-79del
XM_017026989.1:c.706-79del	XP_016882478.1:n.706-79del
XM_017026990.1:c.705+1526del	XP_016882479.1:n.705+1526del
XM_017026991.1:c.*237del	XP_016882480.1:n.*237del
NM_030662.4:c.706-79del MANE Select	NP_109587.1:n.706-79del