Canonical Allele Identifier: CA392936441

Gene: MAP2K1

Linked Data

• dbSNP Id: rs2140668130
• MyVariant Identifiers: chr15:g.66774186A>T (hg19) ; chr15:g.66481848A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66481848A>T , CM000677.2:g.66481848A>T	GRCh38
NC_000015.9:g.66774186A>T , CM000677.1:g.66774186A>T	GRCh37
NC_000015.8:g.64561240A>T	NCBI36
NG_008305.1:g.99976A>T , LRG_725:g.99976A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684779.1:c.596A>T	ENSP00000508681.1:p.Asn199Ile
ENST00000685172.1:c.662A>T	ENSP00000509604.1:p.Asn221Ile
ENST00000685763.1:c.515A>T	ENSP00000509016.1:p.Asn172Ile
ENST00000686347.1:c.569-5380A>T	ENSP00000509027.1:n.569-5380A>T
ENST00000687191.1:n.1020A>T
ENST00000689951.1:c.713A>T	ENSP00000509308.1:p.Asn238Ile
ENST00000691077.1:c.662A>T	ENSP00000509843.1:p.Asn221Ile
ENST00000691576.1:c.569-3146A>T	ENSP00000510066.1:n.569-3146A>T
ENST00000691937.1:c.662A>T	ENSP00000508768.1:p.Asn221Ile
ENST00000692487.1:c.662A>T	ENSP00000509534.1:p.Asn221Ile
ENST00000692683.1:c.596A>T	ENSP00000508437.1:p.Asn199Ile
ENST00000693150.1:c.518A>T	ENSP00000510309.1:p.Asn173Ile
ENST00000307102.10:c.662A>T MANE Select	ENSP00000302486.5:p.Asn221Ile
ENST00000307102.9:c.662A>T	ENSP00000302486.4:p.Asn221Ile
ENST00000566326.1:c.134A>T	ENSP00000456438.1:p.Asn45Ile
NM_002755.3:c.662A>T , LRG_725t1:c.662A>T	NP_002746.1:p.Asn221Ile
XM_011521783.1:c.596A>T	XP_011520085.1:p.Asn199Ile
XM_011521783.3:c.596A>T	XP_011520085.1:p.Asn199Ile
XM_017022411.2:c.584A>T	XP_016877900.1:p.Asn195Ile
XM_017022412.1:c.518A>T	XP_016877901.1:p.Asn173Ile
XM_017022413.1:c.134A>T	XP_016877902.1:p.Asn45Ile
NM_002755.4:c.662A>T MANE Select	NP_002746.1:p.Asn221Ile