Canonical Allele Identifier: CA2319219784
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090687A= , CM000681.2:g.4090687A= GRCh38
NC_000019.9:g.4090685A= , CM000681.1:g.4090685A= GRCh37
NC_000019.8:g.4041685A= NCBI36
NG_007996.1:g.38442T= , LRG_750:g.38442T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1553T=
ENST00000688002.1:n.3265T=
ENST00000688751.1:n.250T=
ENST00000689792.1:n.1018T=
ENST00000262948.10:c.1114T= MANE Select ENSP00000262948.4:p.Ser372=
ENST00000262948.9:c.1114T= ENSP00000262948.3:p.Ser372=
ENST00000394867.8:c.823T= ENSP00000378336.1:p.Ser275=
ENST00000597263.5:n.299T=
ENST00000599021.1:c.224T=
ENST00000600584.5:n.2563T=
ENST00000601786.5:n.1415T=
NM_030662.3:c.1114T= , LRG_750t1:c.1114T= NP_109587.1:p.Ser372=
XM_006722799.2:c.835T= XP_006722862.1:p.Ser279=
XM_011528133.1:c.544T= XP_011526435.1:p.Ser182=
NM_030662.4:c.1114T= MANE Select NP_109587.1:p.Ser372=