Canonical Allele Identifier: CA403386542

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145050198
• MyVariant Identifiers: chr19:g.4099330C>A (hg19) ; chr19:g.4099332C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099332C>A , CM000681.2:g.4099332C>A	GRCh38
NC_000019.9:g.4099330C>A , CM000681.1:g.4099330C>A	GRCh37
NC_000019.8:g.4050330C>A	NCBI36
NG_007996.1:g.29797G>T , LRG_750:g.29797G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1227G>T
ENST00000687128.1:n.1227G>T
ENST00000688002.1:n.1082G>T
ENST00000689792.1:n.692G>T
ENST00000262948.10:c.788G>T MANE Select	ENSP00000262948.4:p.Gly263Val
ENST00000262948.9:c.788G>T	ENSP00000262948.3:p.Gly263Val
ENST00000394867.8:c.497G>T	ENSP00000378336.1:p.Gly166Val
ENST00000593364.5:n.735G>T
ENST00000595715.1:n.603G>T
ENST00000597263.5:n.169+1687G>T
ENST00000599021.1:c.29+1687G>T
ENST00000600584.5:n.1348G>T
ENST00000601786.5:n.1089G>T
NM_030662.3:c.788G>T , LRG_750t1:c.788G>T	NP_109587.1:p.Gly263Val
XM_006722799.2:c.705+1687G>T	XP_006722862.1:n.705+1687G>T
XM_011528133.1:c.218G>T	XP_011526435.1:p.Gly73Val
XM_017026989.1:c.788G>T	XP_016882478.1:p.Gly263Val
XM_017026990.1:c.705+1687G>T	XP_016882479.1:n.705+1687G>T
NM_030662.4:c.788G>T MANE Select	NP_109587.1:p.Gly263Val