Canonical Allele Identifier: CA392936934
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140673855
MyVariant Identifiers: chr15:g.66777347C>G (hg19) chr15:g.66485009C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485009C>G , CM000677.2:g.66485009C>G GRCh38
NC_000015.9:g.66777347C>G , CM000677.1:g.66777347C>G GRCh37
NC_000015.8:g.64564401C>G NCBI36
NG_008305.1:g.103137C>G , LRG_725:g.103137C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2219C>G ENSP00000508681.1:n.628-2219C>G
ENST00000685172.1:c.713C>G ENSP00000509604.1:p.Thr238Ser
ENST00000685763.1:c.566C>G ENSP00000509016.1:p.Thr189Ser
ENST00000686347.1:c.569-2219C>G ENSP00000509027.1:n.569-2219C>G
ENST00000687191.1:n.1071C>G
ENST00000687481.1:n.128C>G
ENST00000689951.1:c.764C>G ENSP00000509308.1:p.Thr255Ser
ENST00000691077.1:c.709C>G ENSP00000509843.1:p.Leu237Val
ENST00000691576.1:c.584C>G ENSP00000510066.1:p.Thr195Ser
ENST00000691937.1:c.713C>G ENSP00000508768.1:p.Thr238Ser
ENST00000692487.1:c.709C>G ENSP00000509534.1:p.Leu237Val
ENST00000692683.1:c.647C>G ENSP00000508437.1:p.Thr216Ser
ENST00000693150.1:c.569C>G ENSP00000510309.1:p.Thr190Ser
ENST00000307102.10:c.713C>G MANE Select ENSP00000302486.5:p.Thr238Ser
ENST00000307102.9:c.713C>G ENSP00000302486.4:p.Thr238Ser
ENST00000566326.1:c.185C>G ENSP00000456438.1:p.Thr62Ser
NM_002755.3:c.713C>G , LRG_725t1:c.713C>G NP_002746.1:p.Thr238Ser
XM_011521783.1:c.647C>G XP_011520085.1:p.Thr216Ser
XM_011521783.3:c.647C>G XP_011520085.1:p.Thr216Ser
XM_017022411.2:c.635C>G XP_016877900.1:p.Thr212Ser
XM_017022412.1:c.569C>G XP_016877901.1:p.Thr190Ser
XM_017022413.1:c.185C>G XP_016877902.1:p.Thr62Ser
NM_002755.4:c.713C>G MANE Select NP_002746.1:p.Thr238Ser
Search 100 bp 5'
Search 100 bp 3'