Canonical Allele Identifier: CA403383095

Gene: MAP2K2

Linked Data

• COSMIC: COSM4520171 ; COSM4520172
• MyVariant Identifiers: chr19:g.4095386C>T (hg19) ; chr19:g.4095388C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095388C>T , CM000681.2:g.4095388C>T	GRCh38
NC_000019.9:g.4095386C>T , CM000681.1:g.4095386C>T	GRCh37
NC_000019.8:g.4046386C>T	NCBI36
NG_007996.1:g.33741G>A , LRG_750:g.33741G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485G>A
ENST00000688002.1:n.3197G>A
ENST00000688751.1:n.182G>A
ENST00000689792.1:n.950G>A
ENST00000262948.10:c.1046G>A MANE Select	ENSP00000262948.4:p.Cys349Tyr
ENST00000262948.9:c.1046G>A	ENSP00000262948.3:p.Cys349Tyr
ENST00000394867.8:c.755G>A	ENSP00000378336.1:p.Cys252Tyr
ENST00000595715.1:n.861G>A
ENST00000597263.5:n.231G>A
ENST00000599021.1:c.156G>A
ENST00000600584.5:n.1606G>A
ENST00000601786.5:n.1347G>A
NM_030662.3:c.1046G>A , LRG_750t1:c.1046G>A	NP_109587.1:p.Cys349Tyr
XM_006722799.2:c.767G>A	XP_006722862.1:p.Cys256Tyr
XM_011528133.1:c.476G>A	XP_011526435.1:p.Cys159Tyr
XM_017026989.1:c.1046G>A	XP_016882478.1:p.Trp349Ter
XM_017026990.1:c.767G>A	XP_016882479.1:p.Trp256Ter
NM_030662.4:c.1046G>A MANE Select	NP_109587.1:p.Cys349Tyr