Canonical Allele Identifier: CA392937445
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777529T>A (hg19) chr15:g.66485191T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485191T>A , CM000677.2:g.66485191T>A GRCh38
NC_000015.9:g.66777529T>A , CM000677.1:g.66777529T>A GRCh37
NC_000015.8:g.64564583T>A NCBI36
NG_008305.1:g.103319T>A , LRG_725:g.103319T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2037T>A ENSP00000508681.1:n.628-2037T>A
ENST00000685172.1:c.895T>A ENSP00000509604.1:p.Ser299Thr
ENST00000685763.1:c.748T>A ENSP00000509016.1:p.Ser250Thr
ENST00000686347.1:c.569-2037T>A ENSP00000509027.1:n.569-2037T>A
ENST00000687191.1:n.1253T>A
ENST00000687481.1:n.310T>A
ENST00000689951.1:c.946T>A ENSP00000509308.1:p.Ser316Thr
ENST00000691077.1:c.*132T>A ENSP00000509843.1:n.*132T>A
ENST00000691576.1:c.766T>A ENSP00000510066.1:p.Ser256Thr
ENST00000691937.1:c.895T>A ENSP00000508768.1:p.Ser299Thr
ENST00000692487.1:c.*132T>A ENSP00000509534.1:n.*132T>A
ENST00000692683.1:c.829T>A ENSP00000508437.1:p.Ser277Thr
ENST00000693150.1:c.751T>A ENSP00000510309.1:p.Ser251Thr
ENST00000307102.10:c.895T>A MANE Select ENSP00000302486.5:p.Ser299Thr
ENST00000307102.9:c.895T>A ENSP00000302486.4:p.Ser299Thr
ENST00000566326.1:c.367T>A ENSP00000456438.1:p.Ser123Thr
NM_002755.3:c.895T>A , LRG_725t1:c.895T>A NP_002746.1:p.Ser299Thr
XM_011521783.1:c.829T>A XP_011520085.1:p.Ser277Thr
XM_011521783.3:c.829T>A XP_011520085.1:p.Ser277Thr
XM_017022411.2:c.817T>A XP_016877900.1:p.Ser273Thr
XM_017022412.1:c.751T>A XP_016877901.1:p.Ser251Thr
XM_017022413.1:c.367T>A XP_016877902.1:p.Ser123Thr
NM_002755.4:c.895T>A MANE Select NP_002746.1:p.Ser299Thr
Search 100 bp 5'
Search 100 bp 3'