Canonical Allele Identifier: CA392937370
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140675286
MyVariant Identifiers: chr15:g.66777491C>T (hg19) chr15:g.66485153C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485153C>T , CM000677.2:g.66485153C>T GRCh38
NC_000015.9:g.66777491C>T , CM000677.1:g.66777491C>T GRCh37
NC_000015.8:g.64564545C>T NCBI36
NG_008305.1:g.103281C>T , LRG_725:g.103281C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2075C>T ENSP00000508681.1:n.628-2075C>T
ENST00000685172.1:c.857C>T ENSP00000509604.1:p.Thr286Ile
ENST00000685763.1:c.710C>T ENSP00000509016.1:p.Thr237Ile
ENST00000686347.1:c.569-2075C>T ENSP00000509027.1:n.569-2075C>T
ENST00000687191.1:n.1215C>T
ENST00000687481.1:n.272C>T
ENST00000689951.1:c.908C>T ENSP00000509308.1:p.Thr303Ile
ENST00000691077.1:c.*94C>T ENSP00000509843.1:n.*94C>T
ENST00000691576.1:c.728C>T ENSP00000510066.1:p.Thr243Ile
ENST00000691937.1:c.857C>T ENSP00000508768.1:p.Thr286Ile
ENST00000692487.1:c.*94C>T ENSP00000509534.1:n.*94C>T
ENST00000692683.1:c.791C>T ENSP00000508437.1:p.Thr264Ile
ENST00000693150.1:c.713C>T ENSP00000510309.1:p.Thr238Ile
ENST00000307102.10:c.857C>T MANE Select ENSP00000302486.5:p.Thr286Ile
ENST00000307102.9:c.857C>T ENSP00000302486.4:p.Thr286Ile
ENST00000566326.1:c.329C>T ENSP00000456438.1:p.Thr110Ile
NM_002755.3:c.857C>T , LRG_725t1:c.857C>T NP_002746.1:p.Thr286Ile
XM_011521783.1:c.791C>T XP_011520085.1:p.Thr264Ile
XM_011521783.3:c.791C>T XP_011520085.1:p.Thr264Ile
XM_017022411.2:c.779C>T XP_016877900.1:p.Thr260Ile
XM_017022412.1:c.713C>T XP_016877901.1:p.Thr238Ile
XM_017022413.1:c.329C>T XP_016877902.1:p.Thr110Ile
NM_002755.4:c.857C>T MANE Select NP_002746.1:p.Thr286Ile
Search 100 bp 5'
Search 100 bp 3'