Canonical Allele Identifier: CA403392481
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4117460T>G , CM000681.2:g.4117460T>G GRCh38
NC_000019.9:g.4117458T>G , CM000681.1:g.4117458T>G GRCh37
NC_000019.8:g.4068458T>G NCBI36
NG_007996.1:g.11669A>C , LRG_750:g.11669A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000394867.9:n.701A>C
ENST00000687128.1:n.701A>C
ENST00000262948.10:c.262A>C MANE Select ENSP00000262948.4:p.Lys88Gln
ENST00000262948.9:c.262A>C ENSP00000262948.3:p.Lys88Gln
ENST00000394867.8:c.-30A>C ENSP00000378336.1:n.-30A>C
ENST00000599345.1:n.459A>C
NM_030662.3:c.262A>C , LRG_750t1:c.262A>C NP_109587.1:p.Lys88Gln
XM_006722799.2:c.262A>C XP_006722862.1:p.Lys88Gln
XM_017026989.1:c.262A>C XP_016882478.1:p.Lys88Gln
XM_017026990.1:c.262A>C XP_016882479.1:p.Lys88Gln
XM_017026991.1:c.262A>C XP_016882480.1:p.Lys88Gln
NM_030662.4:c.262A>C MANE Select NP_109587.1:p.Lys88Gln