Canonical Allele Identifier: CA2584878400

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099183-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099184del , CM000681.2:g.4099184del	GRCh38
NC_000019.9:g.4099182del , CM000681.1:g.4099182del	GRCh37
NC_000019.8:g.4050182del	NCBI36
NG_007996.1:g.29945del , LRG_750:g.29945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+17del
ENST00000687128.1:n.1375del
ENST00000688002.1:n.1230del
ENST00000689792.1:n.823+17del
ENST00000262948.10:c.919+17del MANE Select	ENSP00000262948.4:n.919+17del
ENST00000262948.9:c.919+17del	ENSP00000262948.3:n.919+17del
ENST00000394867.8:c.628+17del	ENSP00000378336.1:n.628+17del
ENST00000595715.1:n.734+17del
ENST00000597263.5:n.169+1835del
ENST00000599021.1:c.29+1835del
ENST00000600584.5:n.1479+17del
ENST00000601786.5:n.1220+17del
NM_030662.3:c.919+17del , LRG_750t1:c.919+17del	NP_109587.1:n.919+17del
XM_006722799.2:c.705+1835del	XP_006722862.1:n.705+1835del
XM_011528133.1:c.349+17del	XP_011526435.1:n.349+17del
XM_017026989.1:c.919+17del	XP_016882478.1:n.919+17del
XM_017026990.1:c.705+1835del	XP_016882479.1:n.705+1835del
NM_030662.4:c.919+17del MANE Select	NP_109587.1:n.919+17del