Canonical Allele Identifier: CA403392473
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4117457C>T , CM000681.2:g.4117457C>T GRCh38
NC_000019.9:g.4117455C>T , CM000681.1:g.4117455C>T GRCh37
NC_000019.8:g.4068455C>T NCBI36
NG_007996.1:g.11672G>A , LRG_750:g.11672G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394867.9:n.704G>A
ENST00000687128.1:n.704G>A
ENST00000262948.10:c.265G>A MANE Select ENSP00000262948.4:p.Val89Ile
ENST00000262948.9:c.265G>A ENSP00000262948.3:p.Val89Ile
ENST00000394867.8:c.-27G>A ENSP00000378336.1:n.-27G>A
ENST00000599345.1:n.462G>A
NM_030662.3:c.265G>A , LRG_750t1:c.265G>A NP_109587.1:p.Val89Ile
XM_006722799.2:c.265G>A XP_006722862.1:p.Val89Ile
XM_017026989.1:c.265G>A XP_016882478.1:p.Val89Ile
XM_017026990.1:c.265G>A XP_016882479.1:p.Val89Ile
XM_017026991.1:c.265G>A XP_016882480.1:p.Val89Ile
NM_030662.4:c.265G>A MANE Select NP_109587.1:p.Val89Ile