Canonical Allele Identifier: CA403387970

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145050556
• COSMIC: COSM5365233 ; COSM5365234
• MyVariant Identifiers: chr19:g.4099408T>A (hg19) ; chr19:g.4099410T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099410T>A , CM000681.2:g.4099410T>A	GRCh38
NC_000019.9:g.4099408T>A , CM000681.1:g.4099408T>A	GRCh37
NC_000019.8:g.4050408T>A	NCBI36
NG_007996.1:g.29719A>T , LRG_750:g.29719A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1149A>T
ENST00000687128.1:n.1149A>T
ENST00000688002.1:n.1004A>T
ENST00000689792.1:n.646-32A>T
ENST00000262948.10:c.710A>T MANE Select	ENSP00000262948.4:p.Glu237Val
ENST00000262948.9:c.710A>T	ENSP00000262948.3:p.Glu237Val
ENST00000394867.8:c.419A>T	ENSP00000378336.1:p.Glu140Val
ENST00000593364.5:n.657A>T
ENST00000595715.1:n.525A>T
ENST00000597263.5:n.169+1609A>T
ENST00000599021.1:c.29+1609A>T
ENST00000600584.5:n.1270A>T
ENST00000601786.5:n.1011A>T
ENST00000602167.5:n.430A>T
NM_030662.3:c.710A>T , LRG_750t1:c.710A>T	NP_109587.1:p.Glu237Val
XM_006722799.2:c.705+1609A>T	XP_006722862.1:n.705+1609A>T
XM_011528133.1:c.140A>T	XP_011526435.1:p.Glu47Val
XM_017026989.1:c.710A>T	XP_016882478.1:p.Glu237Val
XM_017026990.1:c.705+1609A>T	XP_016882479.1:n.705+1609A>T
NM_030662.4:c.710A>T MANE Select	NP_109587.1:p.Glu237Val