Canonical Allele Identifier: CA392937264
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777444G>T (hg19) chr15:g.66485106G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485106G>T , CM000677.2:g.66485106G>T GRCh38
NC_000015.9:g.66777444G>T , CM000677.1:g.66777444G>T GRCh37
NC_000015.8:g.64564498G>T NCBI36
NG_008305.1:g.103234G>T , LRG_725:g.103234G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2122G>T ENSP00000508681.1:n.628-2122G>T
ENST00000685172.1:c.810G>T ENSP00000509604.1:p.Glu270Asp
ENST00000685763.1:c.663G>T ENSP00000509016.1:p.Glu221Asp
ENST00000686347.1:c.569-2122G>T ENSP00000509027.1:n.569-2122G>T
ENST00000687191.1:n.1168G>T
ENST00000687481.1:n.225G>T
ENST00000689951.1:c.861G>T ENSP00000509308.1:p.Glu287Asp
ENST00000691077.1:c.*47G>T ENSP00000509843.1:n.*47G>T
ENST00000691576.1:c.681G>T ENSP00000510066.1:p.Glu227Asp
ENST00000691937.1:c.810G>T ENSP00000508768.1:p.Glu270Asp
ENST00000692487.1:c.*47G>T ENSP00000509534.1:n.*47G>T
ENST00000692683.1:c.744G>T ENSP00000508437.1:p.Glu248Asp
ENST00000693150.1:c.666G>T ENSP00000510309.1:p.Glu222Asp
ENST00000307102.10:c.810G>T MANE Select ENSP00000302486.5:p.Glu270Asp
ENST00000307102.9:c.810G>T ENSP00000302486.4:p.Glu270Asp
ENST00000566326.1:c.282G>T ENSP00000456438.1:p.Glu94Asp
NM_002755.3:c.810G>T , LRG_725t1:c.810G>T NP_002746.1:p.Glu270Asp
XM_011521783.1:c.744G>T XP_011520085.1:p.Glu248Asp
XM_011521783.3:c.744G>T XP_011520085.1:p.Glu248Asp
XM_017022411.2:c.732G>T XP_016877900.1:p.Glu244Asp
XM_017022412.1:c.666G>T XP_016877901.1:p.Glu222Asp
XM_017022413.1:c.282G>T XP_016877902.1:p.Glu94Asp
NM_002755.4:c.810G>T MANE Select NP_002746.1:p.Glu270Asp
Search 100 bp 5'
Search 100 bp 3'