Canonical Allele Identifier: CA392937150
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140674615
MyVariant Identifiers: chr15:g.66777414G>T (hg19) chr15:g.66485076G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485076G>T , CM000677.2:g.66485076G>T GRCh38
NC_000015.9:g.66777414G>T , CM000677.1:g.66777414G>T GRCh37
NC_000015.8:g.64564468G>T NCBI36
NG_008305.1:g.103204G>T , LRG_725:g.103204G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2152G>T ENSP00000508681.1:n.628-2152G>T
ENST00000685172.1:c.780G>T ENSP00000509604.1:p.Arg260Ser
ENST00000685763.1:c.633G>T ENSP00000509016.1:p.Arg211Ser
ENST00000686347.1:c.569-2152G>T ENSP00000509027.1:n.569-2152G>T
ENST00000687191.1:n.1138G>T
ENST00000687481.1:n.195G>T
ENST00000689951.1:c.831G>T ENSP00000509308.1:p.Arg277Ser
ENST00000691077.1:c.*17G>T ENSP00000509843.1:n.*17G>T
ENST00000691576.1:c.651G>T ENSP00000510066.1:p.Arg217Ser
ENST00000691937.1:c.780G>T ENSP00000508768.1:p.Arg260Ser
ENST00000692487.1:c.*17G>T ENSP00000509534.1:n.*17G>T
ENST00000692683.1:c.714G>T ENSP00000508437.1:p.Arg238Ser
ENST00000693150.1:c.636G>T ENSP00000510309.1:p.Arg212Ser
ENST00000307102.10:c.780G>T MANE Select ENSP00000302486.5:p.Arg260Ser
ENST00000307102.9:c.780G>T ENSP00000302486.4:p.Arg260Ser
ENST00000566326.1:c.252G>T ENSP00000456438.1:p.Arg84Ser
NM_002755.3:c.780G>T , LRG_725t1:c.780G>T NP_002746.1:p.Arg260Ser
XM_011521783.1:c.714G>T XP_011520085.1:p.Arg238Ser
XM_011521783.3:c.714G>T XP_011520085.1:p.Arg238Ser
XM_017022411.2:c.702G>T XP_016877900.1:p.Arg234Ser
XM_017022412.1:c.636G>T XP_016877901.1:p.Arg212Ser
XM_017022413.1:c.252G>T XP_016877902.1:p.Arg84Ser
NM_002755.4:c.780G>T MANE Select NP_002746.1:p.Arg260Ser
Search 100 bp 5'
Search 100 bp 3'