Canonical Allele Identifier: CA2319230682
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4110383A= , CM000681.2:g.4110383A= GRCh38
NC_000019.9:g.4110381A= , CM000681.1:g.4110381A= GRCh37
NC_000019.8:g.4061381A= NCBI36
NG_007996.1:g.18746T= , LRG_750:g.18746T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.889+126T=
ENST00000687128.1:n.889+126T=
ENST00000262948.10:c.450+126T= MANE Select ENSP00000262948.4:n.450+126T=
ENST00000262948.9:c.450+126T= ENSP00000262948.3:n.450+126T=
ENST00000394867.8:c.159+126T= ENSP00000378336.1:n.159+126T=
ENST00000599345.1:n.647+126T=
NM_030662.3:c.450+126T= , LRG_750t1:c.450+126T= NP_109587.1:n.450+126T=
XM_006722799.2:c.450+126T= XP_006722862.1:n.450+126T=
XM_017026989.1:c.450+126T= XP_016882478.1:n.450+126T=
XM_017026990.1:c.450+126T= XP_016882479.1:n.450+126T=
XM_017026991.1:c.450+126T= XP_016882480.1:n.450+126T=
NM_030662.4:c.450+126T= MANE Select NP_109587.1:n.450+126T=