Canonical Allele Identifier: CA392936405
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140668030
MyVariant Identifiers: chr15:g.66774177C>A (hg19) chr15:g.66481839C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481839C>A , CM000677.2:g.66481839C>A GRCh38
NC_000015.9:g.66774177C>A , CM000677.1:g.66774177C>A GRCh37
NC_000015.8:g.64561231C>A NCBI36
NG_008305.1:g.99967C>A , LRG_725:g.99967C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.587C>A ENSP00000508681.1:p.Ser196Tyr
ENST00000685172.1:c.653C>A ENSP00000509604.1:p.Ser218Tyr
ENST00000685763.1:c.506C>A ENSP00000509016.1:p.Ser169Tyr
ENST00000686347.1:c.569-5389C>A ENSP00000509027.1:n.569-5389C>A
ENST00000687191.1:n.1011C>A
ENST00000689951.1:c.704C>A ENSP00000509308.1:p.Ser235Tyr
ENST00000691077.1:c.653C>A ENSP00000509843.1:p.Ser218Tyr
ENST00000691576.1:c.569-3155C>A ENSP00000510066.1:n.569-3155C>A
ENST00000691937.1:c.653C>A ENSP00000508768.1:p.Ser218Tyr
ENST00000692487.1:c.653C>A ENSP00000509534.1:p.Ser218Tyr
ENST00000692683.1:c.587C>A ENSP00000508437.1:p.Ser196Tyr
ENST00000693150.1:c.509C>A ENSP00000510309.1:p.Ser170Tyr
ENST00000307102.10:c.653C>A MANE Select ENSP00000302486.5:p.Ser218Tyr
ENST00000307102.9:c.653C>A ENSP00000302486.4:p.Ser218Tyr
ENST00000566326.1:c.125C>A ENSP00000456438.1:p.Ser42Tyr
NM_002755.3:c.653C>A , LRG_725t1:c.653C>A NP_002746.1:p.Ser218Tyr
XM_011521783.1:c.587C>A XP_011520085.1:p.Ser196Tyr
XM_011521783.3:c.587C>A XP_011520085.1:p.Ser196Tyr
XM_017022411.2:c.575C>A XP_016877900.1:p.Ser192Tyr
XM_017022412.1:c.509C>A XP_016877901.1:p.Ser170Tyr
XM_017022413.1:c.125C>A XP_016877902.1:p.Ser42Tyr
NM_002755.4:c.653C>A MANE Select NP_002746.1:p.Ser218Tyr
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