Canonical Allele Identifier: CA2584878590

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099512-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099512G>A , CM000681.2:g.4099512G>A	GRCh38
NC_000019.9:g.4099510G>A , CM000681.1:g.4099510G>A	GRCh37
NC_000019.8:g.4050510G>A	NCBI36
NG_007996.1:g.29617C>T , LRG_750:g.29617C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-98C>T
ENST00000687128.1:n.1145-98C>T
ENST00000688002.1:n.902C>T
ENST00000689792.1:n.646-134C>T
ENST00000262948.10:c.706-98C>T MANE Select	ENSP00000262948.4:n.706-98C>T
ENST00000262948.9:c.706-98C>T	ENSP00000262948.3:n.706-98C>T
ENST00000394867.8:c.415-98C>T	ENSP00000378336.1:n.415-98C>T
ENST00000593364.5:n.653-98C>T
ENST00000595715.1:n.423C>T
ENST00000597263.5:n.169+1507C>T
ENST00000599021.1:c.29+1507C>T
ENST00000600584.5:n.1168C>T
ENST00000601786.5:n.1007-98C>T
ENST00000602167.5:n.426-98C>T
NM_030662.3:c.706-98C>T , LRG_750t1:c.706-98C>T	NP_109587.1:n.706-98C>T
XM_006722799.2:c.705+1507C>T	XP_006722862.1:n.705+1507C>T
XM_011528133.1:c.136-98C>T	XP_011526435.1:n.136-98C>T
XM_017026989.1:c.706-98C>T	XP_016882478.1:n.706-98C>T
XM_017026990.1:c.705+1507C>T	XP_016882479.1:n.705+1507C>T
XM_017026991.1:c.*218C>T	XP_016882480.1:n.*218C>T
NM_030662.4:c.706-98C>T MANE Select	NP_109587.1:n.706-98C>T