Canonical Allele Identifier: CA403380820
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090636G>C , CM000681.2:g.4090636G>C GRCh38
NC_000019.9:g.4090634G>C , CM000681.1:g.4090634G>C GRCh37
NC_000019.8:g.4041634G>C NCBI36
NG_007996.1:g.38493C>G , LRG_750:g.38493C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1604C>G
ENST00000688002.1:n.3316C>G
ENST00000688751.1:n.301C>G
ENST00000689792.1:n.1069C>G
ENST00000262948.10:c.1165C>G MANE Select ENSP00000262948.4:p.Leu389Val
ENST00000262948.9:c.1165C>G ENSP00000262948.3:p.Leu389Val
ENST00000394867.8:c.874C>G ENSP00000378336.1:p.Leu292Val
ENST00000597263.5:n.350C>G
ENST00000599021.1:c.275C>G
ENST00000600584.5:n.2614C>G
ENST00000601786.5:n.1466C>G
NM_030662.3:c.1165C>G , LRG_750t1:c.1165C>G NP_109587.1:p.Leu389Val
XM_006722799.2:c.886C>G XP_006722862.1:p.Leu296Val
XM_011528133.1:c.595C>G XP_011526435.1:p.Leu199Val
NM_030662.4:c.1165C>G MANE Select NP_109587.1:p.Leu389Val