Canonical Allele Identifier: CA392937355
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777484G>T (hg19) chr15:g.66485146G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485146G>T , CM000677.2:g.66485146G>T GRCh38
NC_000015.9:g.66777484G>T , CM000677.1:g.66777484G>T GRCh37
NC_000015.8:g.64564538G>T NCBI36
NG_008305.1:g.103274G>T , LRG_725:g.103274G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2082G>T ENSP00000508681.1:n.628-2082G>T
ENST00000685172.1:c.850G>T ENSP00000509604.1:p.Ala284Ser
ENST00000685763.1:c.703G>T ENSP00000509016.1:p.Ala235Ser
ENST00000686347.1:c.569-2082G>T ENSP00000509027.1:n.569-2082G>T
ENST00000687191.1:n.1208G>T
ENST00000687481.1:n.265G>T
ENST00000689951.1:c.901G>T ENSP00000509308.1:p.Ala301Ser
ENST00000691077.1:c.*87G>T ENSP00000509843.1:n.*87G>T
ENST00000691576.1:c.721G>T ENSP00000510066.1:p.Ala241Ser
ENST00000691937.1:c.850G>T ENSP00000508768.1:p.Ala284Ser
ENST00000692487.1:c.*87G>T ENSP00000509534.1:n.*87G>T
ENST00000692683.1:c.784G>T ENSP00000508437.1:p.Ala262Ser
ENST00000693150.1:c.706G>T ENSP00000510309.1:p.Ala236Ser
ENST00000307102.10:c.850G>T MANE Select ENSP00000302486.5:p.Ala284Ser
ENST00000307102.9:c.850G>T ENSP00000302486.4:p.Ala284Ser
ENST00000566326.1:c.322G>T ENSP00000456438.1:p.Ala108Ser
NM_002755.3:c.850G>T , LRG_725t1:c.850G>T NP_002746.1:p.Ala284Ser
XM_011521783.1:c.784G>T XP_011520085.1:p.Ala262Ser
XM_011521783.3:c.784G>T XP_011520085.1:p.Ala262Ser
XM_017022411.2:c.772G>T XP_016877900.1:p.Ala258Ser
XM_017022412.1:c.706G>T XP_016877901.1:p.Ala236Ser
XM_017022413.1:c.322G>T XP_016877902.1:p.Ala108Ser
NM_002755.4:c.850G>T MANE Select NP_002746.1:p.Ala284Ser
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