Canonical Allele Identifier: CA392937063
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140674322
gnomAD v4: 15-66485056-G-T
MyVariant Identifiers: chr15:g.66777394G>T (hg19) chr15:g.66485056G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485056G>T , CM000677.2:g.66485056G>T GRCh38
NC_000015.9:g.66777394G>T , CM000677.1:g.66777394G>T GRCh37
NC_000015.8:g.64564448G>T NCBI36
NG_008305.1:g.103184G>T , LRG_725:g.103184G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2172G>T ENSP00000508681.1:n.628-2172G>T
ENST00000685172.1:c.760G>T ENSP00000509604.1:p.Val254Leu
ENST00000685763.1:c.613G>T ENSP00000509016.1:p.Val205Leu
ENST00000686347.1:c.569-2172G>T ENSP00000509027.1:n.569-2172G>T
ENST00000687191.1:n.1118G>T
ENST00000687481.1:n.175G>T
ENST00000689951.1:c.811G>T ENSP00000509308.1:p.Val271Leu
ENST00000691077.1:c.756G>T ENSP00000509843.1:p.Trp252Cys
ENST00000691576.1:c.631G>T ENSP00000510066.1:p.Val211Leu
ENST00000691937.1:c.760G>T ENSP00000508768.1:p.Val254Leu
ENST00000692487.1:c.756G>T ENSP00000509534.1:p.Trp252Cys
ENST00000692683.1:c.694G>T ENSP00000508437.1:p.Val232Leu
ENST00000693150.1:c.616G>T ENSP00000510309.1:p.Val206Leu
ENST00000307102.10:c.760G>T MANE Select ENSP00000302486.5:p.Val254Leu
ENST00000307102.9:c.760G>T ENSP00000302486.4:p.Val254Leu
ENST00000566326.1:c.232G>T ENSP00000456438.1:p.Val78Leu
NM_002755.3:c.760G>T , LRG_725t1:c.760G>T NP_002746.1:p.Val254Leu
XM_011521783.1:c.694G>T XP_011520085.1:p.Val232Leu
XM_011521783.3:c.694G>T XP_011520085.1:p.Val232Leu
XM_017022411.2:c.682G>T XP_016877900.1:p.Val228Leu
XM_017022412.1:c.616G>T XP_016877901.1:p.Val206Leu
XM_017022413.1:c.232G>T XP_016877902.1:p.Val78Leu
NM_002755.4:c.760G>T MANE Select NP_002746.1:p.Val254Leu
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