Canonical Allele Identifier: CA392936933
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777347C>A (hg19) chr15:g.66485009C>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2219C>A ENSP00000508681.1:n.628-2219C>A
ENST00000685172.1:c.713C>A ENSP00000509604.1:p.Thr238Asn
ENST00000685763.1:c.566C>A ENSP00000509016.1:p.Thr189Asn
ENST00000686347.1:c.569-2219C>A ENSP00000509027.1:n.569-2219C>A
ENST00000687191.1:n.1071C>A
ENST00000687481.1:n.128C>A
ENST00000689951.1:c.764C>A ENSP00000509308.1:p.Thr255Asn
ENST00000691077.1:c.709C>A ENSP00000509843.1:p.Leu237Ile
ENST00000691576.1:c.584C>A ENSP00000510066.1:p.Thr195Asn
ENST00000691937.1:c.713C>A ENSP00000508768.1:p.Thr238Asn
ENST00000692487.1:c.709C>A ENSP00000509534.1:p.Leu237Ile
ENST00000692683.1:c.647C>A ENSP00000508437.1:p.Thr216Asn
ENST00000693150.1:c.569C>A ENSP00000510309.1:p.Thr190Asn
ENST00000307102.10:c.713C>A MANE Select ENSP00000302486.5:p.Thr238Asn
ENST00000307102.9:c.713C>A ENSP00000302486.4:p.Thr238Asn
ENST00000566326.1:c.185C>A ENSP00000456438.1:p.Thr62Asn
NM_002755.3:c.713C>A , LRG_725t1:c.713C>A NP_002746.1:p.Thr238Asn
XM_011521783.1:c.647C>A XP_011520085.1:p.Thr216Asn
XM_011521783.3:c.647C>A XP_011520085.1:p.Thr216Asn
XM_017022411.2:c.635C>A XP_016877900.1:p.Thr212Asn
XM_017022412.1:c.569C>A XP_016877901.1:p.Thr190Asn
XM_017022413.1:c.185C>A XP_016877902.1:p.Thr62Asn
NM_002755.4:c.713C>A MANE Select NP_002746.1:p.Thr238Asn
Search 100 bp 5'
Search 100 bp 3'