Canonical Allele Identifier: CA490858526
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777438C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485100C>T , CM000677.2:g.66485100C>T GRCh38
NC_000015.9:g.66777438C>T , CM000677.1:g.66777438C>T GRCh37
NC_000015.8:g.64564492C>T NCBI36
NG_008305.1:g.103228C>T , LRG_725:g.103228C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2128C>T ENSP00000508681.1:n.628-2128C>T
ENST00000685172.1:c.804C>T ENSP00000509604.1:p.Ala268=
ENST00000685763.1:c.657C>T ENSP00000509016.1:p.Ala219=
ENST00000686347.1:c.569-2128C>T ENSP00000509027.1:n.569-2128C>T
ENST00000687191.1:n.1162C>T
ENST00000687481.1:n.219C>T
ENST00000689951.1:c.855C>T ENSP00000509308.1:p.Ala285=
ENST00000691077.1:c.*41C>T ENSP00000509843.1:n.*41C>T
ENST00000691576.1:c.675C>T ENSP00000510066.1:p.Ala225=
ENST00000691937.1:c.804C>T ENSP00000508768.1:p.Ala268=
ENST00000692487.1:c.*41C>T ENSP00000509534.1:n.*41C>T
ENST00000692683.1:c.738C>T ENSP00000508437.1:p.Ala246=
ENST00000693150.1:c.660C>T ENSP00000510309.1:p.Ala220=
ENST00000307102.10:c.804C>T MANE Select ENSP00000302486.5:p.Ala268=
ENST00000307102.9:c.804C>T ENSP00000302486.4:p.Ala268=
ENST00000566326.1:c.276C>T ENSP00000456438.1:p.Ala92=
NM_002755.3:c.804C>T , LRG_725t1:c.804C>T NP_002746.1:p.Ala268=
XM_011521783.1:c.738C>T XP_011520085.1:p.Ala246=
XM_011521783.3:c.738C>T XP_011520085.1:p.Ala246=
XM_017022411.2:c.726C>T XP_016877900.1:p.Ala242=
XM_017022412.1:c.660C>T XP_016877901.1:p.Ala220=
XM_017022413.1:c.276C>T XP_016877902.1:p.Ala92=
NM_002755.4:c.804C>T MANE Select NP_002746.1:p.Ala268=
Search 100 bp 5'
Search 100 bp 3'