Canonical Allele Identifier: CA392937341
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777478G>T (hg19) chr15:g.66485140G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485140G>T , CM000677.2:g.66485140G>T GRCh38
NC_000015.9:g.66777478G>T , CM000677.1:g.66777478G>T GRCh37
NC_000015.8:g.64564532G>T NCBI36
NG_008305.1:g.103268G>T , LRG_725:g.103268G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2088G>T ENSP00000508681.1:n.628-2088G>T
ENST00000685172.1:c.844G>T ENSP00000509604.1:p.Asp282Tyr
ENST00000685763.1:c.697G>T ENSP00000509016.1:p.Asp233Tyr
ENST00000686347.1:c.569-2088G>T ENSP00000509027.1:n.569-2088G>T
ENST00000687191.1:n.1202G>T
ENST00000687481.1:n.259G>T
ENST00000689951.1:c.895G>T ENSP00000509308.1:p.Asp299Tyr
ENST00000691077.1:c.*81G>T ENSP00000509843.1:n.*81G>T
ENST00000691576.1:c.715G>T ENSP00000510066.1:p.Asp239Tyr
ENST00000691937.1:c.844G>T ENSP00000508768.1:p.Asp282Tyr
ENST00000692487.1:c.*81G>T ENSP00000509534.1:n.*81G>T
ENST00000692683.1:c.778G>T ENSP00000508437.1:p.Asp260Tyr
ENST00000693150.1:c.700G>T ENSP00000510309.1:p.Asp234Tyr
ENST00000307102.10:c.844G>T MANE Select ENSP00000302486.5:p.Asp282Tyr
ENST00000307102.9:c.844G>T ENSP00000302486.4:p.Asp282Tyr
ENST00000566326.1:c.316G>T ENSP00000456438.1:p.Asp106Tyr
NM_002755.3:c.844G>T , LRG_725t1:c.844G>T NP_002746.1:p.Asp282Tyr
XM_011521783.1:c.778G>T XP_011520085.1:p.Asp260Tyr
XM_011521783.3:c.778G>T XP_011520085.1:p.Asp260Tyr
XM_017022411.2:c.766G>T XP_016877900.1:p.Asp256Tyr
XM_017022412.1:c.700G>T XP_016877901.1:p.Asp234Tyr
XM_017022413.1:c.316G>T XP_016877902.1:p.Asp106Tyr
NM_002755.4:c.844G>T MANE Select NP_002746.1:p.Asp282Tyr
Search 100 bp 5'
Search 100 bp 3'