Canonical Allele Identifier: CA392936760

Gene: MAP2K1

Linked Data

• MyVariant Identifiers: chr15:g.66777329C>T (hg19) ; chr15:g.66484991C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66484991C>T , CM000677.2:g.66484991C>T	GRCh38
NC_000015.9:g.66777329C>T , CM000677.1:g.66777329C>T	GRCh37
NC_000015.8:g.64564383C>T	NCBI36
NG_008305.1:g.103119C>T , LRG_725:g.103119C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.628-2237C>T	ENSP00000508681.1:n.628-2237C>T
ENST00000685172.1:c.695C>T	ENSP00000509604.1:p.Pro232Leu
ENST00000685763.1:c.548C>T	ENSP00000509016.1:p.Pro183Leu
ENST00000686347.1:c.569-2237C>T	ENSP00000509027.1:n.569-2237C>T
ENST00000687191.1:n.1053C>T
ENST00000687481.1:n.110C>T
ENST00000689951.1:c.746C>T	ENSP00000509308.1:p.Pro249Leu
ENST00000691077.1:c.694-3C>T	ENSP00000509843.1:n.694-3C>T
ENST00000691576.1:c.569-3C>T	ENSP00000510066.1:n.569-3C>T
ENST00000691937.1:c.695C>T	ENSP00000508768.1:p.Pro232Leu
ENST00000692487.1:c.694-3C>T	ENSP00000509534.1:n.694-3C>T
ENST00000692683.1:c.629C>T	ENSP00000508437.1:p.Pro210Leu
ENST00000693150.1:c.551C>T	ENSP00000510309.1:p.Pro184Leu
ENST00000307102.10:c.695C>T MANE Select	ENSP00000302486.5:p.Pro232Leu
ENST00000307102.9:c.695C>T	ENSP00000302486.4:p.Pro232Leu
ENST00000566326.1:c.167C>T	ENSP00000456438.1:p.Pro56Leu
NM_002755.3:c.695C>T , LRG_725t1:c.695C>T	NP_002746.1:p.Pro232Leu
XM_011521783.1:c.629C>T	XP_011520085.1:p.Pro210Leu
XM_011521783.3:c.629C>T	XP_011520085.1:p.Pro210Leu
XM_017022411.2:c.617C>T	XP_016877900.1:p.Pro206Leu
XM_017022412.1:c.551C>T	XP_016877901.1:p.Pro184Leu
XM_017022413.1:c.167C>T	XP_016877902.1:p.Pro56Leu
NM_002755.4:c.695C>T MANE Select	NP_002746.1:p.Pro232Leu