Canonical Allele Identifier: CA392937029
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140674232

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485047C>G , CM000677.2:g.66485047C>G GRCh38
NC_000015.9:g.66777385C>G , CM000677.1:g.66777385C>G GRCh37
NC_000015.8:g.64564439C>G NCBI36
NG_008305.1:g.103175C>G , LRG_725:g.103175C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2181C>G ENSP00000508681.1:n.628-2181C>G
ENST00000685172.1:c.751C>G ENSP00000509604.1:p.Leu251Val
ENST00000685763.1:c.604C>G ENSP00000509016.1:p.Leu202Val
ENST00000686347.1:c.569-2181C>G ENSP00000509027.1:n.569-2181C>G
ENST00000687191.1:n.1109C>G
ENST00000687481.1:n.166C>G
ENST00000689951.1:c.802C>G ENSP00000509308.1:p.Leu268Val
ENST00000691077.1:c.747C>G ENSP00000509843.1:p.Asp249Glu
ENST00000691576.1:c.622C>G ENSP00000510066.1:p.Leu208Val
ENST00000691937.1:c.751C>G ENSP00000508768.1:p.Leu251Val
ENST00000692487.1:c.747C>G ENSP00000509534.1:p.Asp249Glu
ENST00000692683.1:c.685C>G ENSP00000508437.1:p.Leu229Val
ENST00000693150.1:c.607C>G ENSP00000510309.1:p.Leu203Val
ENST00000307102.10:c.751C>G MANE Select ENSP00000302486.5:p.Leu251Val
ENST00000307102.9:c.751C>G ENSP00000302486.4:p.Leu251Val
ENST00000566326.1:c.223C>G ENSP00000456438.1:p.Leu75Val
NM_002755.3:c.751C>G , LRG_725t1:c.751C>G NP_002746.1:p.Leu251Val
XM_011521783.1:c.685C>G XP_011520085.1:p.Leu229Val
XM_011521783.3:c.685C>G XP_011520085.1:p.Leu229Val
XM_017022411.2:c.673C>G XP_016877900.1:p.Leu225Val
XM_017022412.1:c.607C>G XP_016877901.1:p.Leu203Val
XM_017022413.1:c.223C>G XP_016877902.1:p.Leu75Val
NM_002755.4:c.751C>G MANE Select NP_002746.1:p.Leu251Val