Canonical Allele Identifier: CA2840265137

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4110566del , CM000681.2:g.4110566del	GRCh38
NC_000019.9:g.4110564del , CM000681.1:g.4110564del	GRCh37
NC_000019.8:g.4061564del	NCBI36
NG_007996.1:g.18565del , LRG_750:g.18565del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.834del
ENST00000687128.1:n.834del
ENST00000262948.10:c.395del MANE Select	ENSP00000262948.4:p.Gly132AlafsTer28
ENST00000262948.9:c.395del	ENSP00000262948.3:p.Gly132AlafsTer28
ENST00000394867.8:c.104del	ENSP00000378336.1:p.Gly35AlafsTer28
ENST00000599345.1:n.592del
NM_030662.3:c.395del , LRG_750t1:c.395del	NP_109587.1:p.Gly132AlafsTer28
XM_006722799.2:c.395del	XP_006722862.1:p.Gly132AlafsTer28
XM_017026989.1:c.395del	XP_016882478.1:p.Gly132AlafsTer28
XM_017026990.1:c.395del	XP_016882479.1:p.Gly132AlafsTer28
XM_017026991.1:c.395del	XP_016882480.1:p.Gly132AlafsTer28
NM_030662.4:c.395del MANE Select	NP_109587.1:p.Gly132AlafsTer28