Canonical Allele Identifier: CA392936928
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140673802
MyVariant Identifiers: chr15:g.66777344G>T (hg19) chr15:g.66485006G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485006G>T , CM000677.2:g.66485006G>T GRCh38
NC_000015.9:g.66777344G>T , CM000677.1:g.66777344G>T GRCh37
NC_000015.8:g.64564398G>T NCBI36
NG_008305.1:g.103134G>T , LRG_725:g.103134G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2222G>T ENSP00000508681.1:n.628-2222G>T
ENST00000685172.1:c.710G>T ENSP00000509604.1:p.Gly237Val
ENST00000685763.1:c.563G>T ENSP00000509016.1:p.Gly188Val
ENST00000686347.1:c.569-2222G>T ENSP00000509027.1:n.569-2222G>T
ENST00000687191.1:n.1068G>T
ENST00000687481.1:n.125G>T
ENST00000689951.1:c.761G>T ENSP00000509308.1:p.Gly254Val
ENST00000691077.1:c.706G>T ENSP00000509843.1:p.Gly236Ter
ENST00000691576.1:c.581G>T ENSP00000510066.1:p.Gly194Val
ENST00000691937.1:c.710G>T ENSP00000508768.1:p.Gly237Val
ENST00000692487.1:c.706G>T ENSP00000509534.1:p.Gly236Ter
ENST00000692683.1:c.644G>T ENSP00000508437.1:p.Gly215Val
ENST00000693150.1:c.566G>T ENSP00000510309.1:p.Gly189Val
ENST00000307102.10:c.710G>T MANE Select ENSP00000302486.5:p.Gly237Val
ENST00000307102.9:c.710G>T ENSP00000302486.4:p.Gly237Val
ENST00000566326.1:c.182G>T ENSP00000456438.1:p.Gly61Val
NM_002755.3:c.710G>T , LRG_725t1:c.710G>T NP_002746.1:p.Gly237Val
XM_011521783.1:c.644G>T XP_011520085.1:p.Gly215Val
XM_011521783.3:c.644G>T XP_011520085.1:p.Gly215Val
XM_017022411.2:c.632G>T XP_016877900.1:p.Gly211Val
XM_017022412.1:c.566G>T XP_016877901.1:p.Gly189Val
XM_017022413.1:c.182G>T XP_016877902.1:p.Gly61Val
NM_002755.4:c.710G>T MANE Select NP_002746.1:p.Gly237Val
Search 100 bp 5'
Search 100 bp 3'