Canonical Allele Identifier: CA490858551
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777483G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485145G>T , CM000677.2:g.66485145G>T GRCh38
NC_000015.9:g.66777483G>T , CM000677.1:g.66777483G>T GRCh37
NC_000015.8:g.64564537G>T NCBI36
NG_008305.1:g.103273G>T , LRG_725:g.103273G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2083G>T ENSP00000508681.1:n.628-2083G>T
ENST00000685172.1:c.849G>T ENSP00000509604.1:p.Ala283=
ENST00000685763.1:c.702G>T ENSP00000509016.1:p.Ala234=
ENST00000686347.1:c.569-2083G>T ENSP00000509027.1:n.569-2083G>T
ENST00000687191.1:n.1207G>T
ENST00000687481.1:n.264G>T
ENST00000689951.1:c.900G>T ENSP00000509308.1:p.Ala300=
ENST00000691077.1:c.*86G>T ENSP00000509843.1:n.*86G>T
ENST00000691576.1:c.720G>T ENSP00000510066.1:p.Ala240=
ENST00000691937.1:c.849G>T ENSP00000508768.1:p.Ala283=
ENST00000692487.1:c.*86G>T ENSP00000509534.1:n.*86G>T
ENST00000692683.1:c.783G>T ENSP00000508437.1:p.Ala261=
ENST00000693150.1:c.705G>T ENSP00000510309.1:p.Ala235=
ENST00000307102.10:c.849G>T MANE Select ENSP00000302486.5:p.Ala283=
ENST00000307102.9:c.849G>T ENSP00000302486.4:p.Ala283=
ENST00000566326.1:c.321G>T ENSP00000456438.1:p.Ala107=
NM_002755.3:c.849G>T , LRG_725t1:c.849G>T NP_002746.1:p.Ala283=
XM_011521783.1:c.783G>T XP_011520085.1:p.Ala261=
XM_011521783.3:c.783G>T XP_011520085.1:p.Ala261=
XM_017022411.2:c.771G>T XP_016877900.1:p.Ala257=
XM_017022412.1:c.705G>T XP_016877901.1:p.Ala235=
XM_017022413.1:c.321G>T XP_016877902.1:p.Ala107=
NM_002755.4:c.849G>T MANE Select NP_002746.1:p.Ala283=
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