Canonical Allele Identifier: CA392937427
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777520C>G (hg19) chr15:g.66485182C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485182C>G , CM000677.2:g.66485182C>G GRCh38
NC_000015.9:g.66777520C>G , CM000677.1:g.66777520C>G GRCh37
NC_000015.8:g.64564574C>G NCBI36
NG_008305.1:g.103310C>G , LRG_725:g.103310C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2046C>G ENSP00000508681.1:n.628-2046C>G
ENST00000685172.1:c.886C>G ENSP00000509604.1:p.Pro296Ala
ENST00000685763.1:c.739C>G ENSP00000509016.1:p.Pro247Ala
ENST00000686347.1:c.569-2046C>G ENSP00000509027.1:n.569-2046C>G
ENST00000687191.1:n.1244C>G
ENST00000687481.1:n.301C>G
ENST00000689951.1:c.937C>G ENSP00000509308.1:p.Pro313Ala
ENST00000691077.1:c.*123C>G ENSP00000509843.1:n.*123C>G
ENST00000691576.1:c.757C>G ENSP00000510066.1:p.Pro253Ala
ENST00000691937.1:c.886C>G ENSP00000508768.1:p.Pro296Ala
ENST00000692487.1:c.*123C>G ENSP00000509534.1:n.*123C>G
ENST00000692683.1:c.820C>G ENSP00000508437.1:p.Pro274Ala
ENST00000693150.1:c.742C>G ENSP00000510309.1:p.Pro248Ala
ENST00000307102.10:c.886C>G MANE Select ENSP00000302486.5:p.Pro296Ala
ENST00000307102.9:c.886C>G ENSP00000302486.4:p.Pro296Ala
ENST00000566326.1:c.358C>G ENSP00000456438.1:p.Pro120Ala
NM_002755.3:c.886C>G , LRG_725t1:c.886C>G NP_002746.1:p.Pro296Ala
XM_011521783.1:c.820C>G XP_011520085.1:p.Pro274Ala
XM_011521783.3:c.820C>G XP_011520085.1:p.Pro274Ala
XM_017022411.2:c.808C>G XP_016877900.1:p.Pro270Ala
XM_017022412.1:c.742C>G XP_016877901.1:p.Pro248Ala
XM_017022413.1:c.358C>G XP_016877902.1:p.Pro120Ala
NM_002755.4:c.886C>G MANE Select NP_002746.1:p.Pro296Ala
Search 100 bp 5'
Search 100 bp 3'