Canonical Allele Identifier: CA392936387

Gene: MAP2K1

Linked Data

• MyVariant Identifiers: chr15:g.66774173G>T (hg19) ; chr15:g.66481835G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66481835G>T , CM000677.2:g.66481835G>T	GRCh38
NC_000015.9:g.66774173G>T , CM000677.1:g.66774173G>T	GRCh37
NC_000015.8:g.64561227G>T	NCBI36
NG_008305.1:g.99963G>T , LRG_725:g.99963G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684779.1:c.583G>T	ENSP00000508681.1:p.Asp195Tyr
ENST00000685172.1:c.649G>T	ENSP00000509604.1:p.Asp217Tyr
ENST00000685763.1:c.502G>T	ENSP00000509016.1:p.Asp168Tyr
ENST00000686347.1:c.569-5393G>T	ENSP00000509027.1:n.569-5393G>T
ENST00000687191.1:n.1007G>T
ENST00000689951.1:c.700G>T	ENSP00000509308.1:p.Asp234Tyr
ENST00000691077.1:c.649G>T	ENSP00000509843.1:p.Asp217Tyr
ENST00000691576.1:c.569-3159G>T	ENSP00000510066.1:n.569-3159G>T
ENST00000691937.1:c.649G>T	ENSP00000508768.1:p.Asp217Tyr
ENST00000692487.1:c.649G>T	ENSP00000509534.1:p.Asp217Tyr
ENST00000692683.1:c.583G>T	ENSP00000508437.1:p.Asp195Tyr
ENST00000693150.1:c.505G>T	ENSP00000510309.1:p.Asp169Tyr
ENST00000307102.10:c.649G>T MANE Select	ENSP00000302486.5:p.Asp217Tyr
ENST00000307102.9:c.649G>T	ENSP00000302486.4:p.Asp217Tyr
ENST00000566326.1:c.121G>T	ENSP00000456438.1:p.Asp41Tyr
NM_002755.3:c.649G>T , LRG_725t1:c.649G>T	NP_002746.1:p.Asp217Tyr
XM_011521783.1:c.583G>T	XP_011520085.1:p.Asp195Tyr
XM_011521783.3:c.583G>T	XP_011520085.1:p.Asp195Tyr
XM_017022411.2:c.571G>T	XP_016877900.1:p.Asp191Tyr
XM_017022412.1:c.505G>T	XP_016877901.1:p.Asp169Tyr
XM_017022413.1:c.121G>T	XP_016877902.1:p.Asp41Tyr
NM_002755.4:c.649G>T MANE Select	NP_002746.1:p.Asp217Tyr