Canonical Allele Identifier: CA392936040
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140667231
gnomAD v4: 15-66481755-A-T
MyVariant Identifiers: chr15:g.66774093A>T (hg19) chr15:g.66481755A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481755A>T , CM000677.2:g.66481755A>T GRCh38
NC_000015.9:g.66774093A>T , CM000677.1:g.66774093A>T GRCh37
NC_000015.8:g.64561147A>T NCBI36
NG_008305.1:g.99883A>T , LRG_725:g.99883A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.503A>T ENSP00000508681.1:p.Asp168Val
ENST00000685172.1:c.569A>T ENSP00000509604.1:p.Asp190Val
ENST00000685763.1:c.422A>T ENSP00000509016.1:p.Asp141Val
ENST00000686347.1:c.569-5473A>T ENSP00000509027.1:n.569-5473A>T
ENST00000687191.1:n.927A>T
ENST00000689951.1:c.620A>T ENSP00000509308.1:p.Asn207Ile
ENST00000691077.1:c.569A>T ENSP00000509843.1:p.Asp190Val
ENST00000691576.1:c.569-3239A>T ENSP00000510066.1:n.569-3239A>T
ENST00000691937.1:c.569A>T ENSP00000508768.1:p.Asp190Val
ENST00000692487.1:c.569A>T ENSP00000509534.1:p.Asp190Val
ENST00000692683.1:c.503A>T ENSP00000508437.1:p.Asp168Val
ENST00000693150.1:c.425A>T ENSP00000510309.1:p.Asp142Val
ENST00000307102.10:c.569A>T MANE Select ENSP00000302486.5:p.Asp190Val
ENST00000307102.9:c.569A>T ENSP00000302486.4:p.Asp190Val
ENST00000566326.1:c.41A>T ENSP00000456438.1:p.Asn14Ile
NM_002755.3:c.569A>T , LRG_725t1:c.569A>T NP_002746.1:p.Asp190Val
XM_011521783.1:c.503A>T XP_011520085.1:p.Asp168Val
XM_011521783.3:c.503A>T XP_011520085.1:p.Asp168Val
XM_017022411.2:c.491A>T XP_016877900.1:p.Asp164Val
XM_017022412.1:c.425A>T XP_016877901.1:p.Asp142Val
XM_017022413.1:c.41A>T XP_016877902.1:p.Asn14Ile
NM_002755.4:c.569A>T MANE Select NP_002746.1:p.Asp190Val
Search 100 bp 5'
Search 100 bp 3'