Canonical Allele Identifier: CA490858422

Gene: MAP2K1

Linked Data

• MyVariant Identifiers: chr15:g.66774172C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66481834C>A , CM000677.2:g.66481834C>A	GRCh38
NC_000015.9:g.66774172C>A , CM000677.1:g.66774172C>A	GRCh37
NC_000015.8:g.64561226C>A	NCBI36
NG_008305.1:g.99962C>A , LRG_725:g.99962C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684779.1:c.582C>A	ENSP00000508681.1:p.Ile194=
ENST00000685172.1:c.648C>A	ENSP00000509604.1:p.Ile216=
ENST00000685763.1:c.501C>A	ENSP00000509016.1:p.Ile167=
ENST00000686347.1:c.569-5394C>A	ENSP00000509027.1:n.569-5394C>A
ENST00000687191.1:n.1006C>A
ENST00000689951.1:c.699C>A	ENSP00000509308.1:p.Ile233=
ENST00000691077.1:c.648C>A	ENSP00000509843.1:p.Ile216=
ENST00000691576.1:c.569-3160C>A	ENSP00000510066.1:n.569-3160C>A
ENST00000691937.1:c.648C>A	ENSP00000508768.1:p.Ile216=
ENST00000692487.1:c.648C>A	ENSP00000509534.1:p.Ile216=
ENST00000692683.1:c.582C>A	ENSP00000508437.1:p.Ile194=
ENST00000693150.1:c.504C>A	ENSP00000510309.1:p.Ile168=
ENST00000307102.10:c.648C>A MANE Select	ENSP00000302486.5:p.Ile216=
ENST00000307102.9:c.648C>A	ENSP00000302486.4:p.Ile216=
ENST00000566326.1:c.120C>A	ENSP00000456438.1:p.Ile40=
NM_002755.3:c.648C>A , LRG_725t1:c.648C>A	NP_002746.1:p.Ile216=
XM_011521783.1:c.582C>A	XP_011520085.1:p.Ile194=
XM_011521783.3:c.582C>A	XP_011520085.1:p.Ile194=
XM_017022411.2:c.570C>A	XP_016877900.1:p.Ile190=
XM_017022412.1:c.504C>A	XP_016877901.1:p.Ile168=
XM_017022413.1:c.120C>A	XP_016877902.1:p.Ile40=
NM_002755.4:c.648C>A MANE Select	NP_002746.1:p.Ile216=