Canonical Allele Identifier: CA392936107
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140667354
MyVariant Identifiers: chr15:g.66774108A>C (hg19) chr15:g.66481770A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481770A>C , CM000677.2:g.66481770A>C GRCh38
NC_000015.9:g.66774108A>C , CM000677.1:g.66774108A>C GRCh37
NC_000015.8:g.64561162A>C NCBI36
NG_008305.1:g.99898A>C , LRG_725:g.99898A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.518A>C ENSP00000508681.1:p.Asn173Thr
ENST00000685172.1:c.584A>C ENSP00000509604.1:p.Asn195Thr
ENST00000685763.1:c.437A>C ENSP00000509016.1:p.Asn146Thr
ENST00000686347.1:c.569-5458A>C ENSP00000509027.1:n.569-5458A>C
ENST00000687191.1:n.942A>C
ENST00000689951.1:c.635A>C ENSP00000509308.1:p.Asn212Thr
ENST00000691077.1:c.584A>C ENSP00000509843.1:p.Asn195Thr
ENST00000691576.1:c.569-3224A>C ENSP00000510066.1:n.569-3224A>C
ENST00000691937.1:c.584A>C ENSP00000508768.1:p.Asn195Thr
ENST00000692487.1:c.584A>C ENSP00000509534.1:p.Asn195Thr
ENST00000692683.1:c.518A>C ENSP00000508437.1:p.Asn173Thr
ENST00000693150.1:c.440A>C ENSP00000510309.1:p.Asn147Thr
ENST00000307102.10:c.584A>C MANE Select ENSP00000302486.5:p.Asn195Thr
ENST00000307102.9:c.584A>C ENSP00000302486.4:p.Asn195Thr
ENST00000566326.1:c.56A>C ENSP00000456438.1:p.Asn19Thr
NM_002755.3:c.584A>C , LRG_725t1:c.584A>C NP_002746.1:p.Asn195Thr
XM_011521783.1:c.518A>C XP_011520085.1:p.Asn173Thr
XM_011521783.3:c.518A>C XP_011520085.1:p.Asn173Thr
XM_017022411.2:c.506A>C XP_016877900.1:p.Asn169Thr
XM_017022412.1:c.440A>C XP_016877901.1:p.Asn147Thr
XM_017022413.1:c.56A>C XP_016877902.1:p.Asn19Thr
NM_002755.4:c.584A>C MANE Select NP_002746.1:p.Asn195Thr
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