Canonical Allele Identifier: CA403386813

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2040968174
• COSMIC: COSM5609280 ; COSM5609281
• MyVariant Identifiers: chr19:g.4099373C>T (hg19) ; chr19:g.4099375C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099375C>T , CM000681.2:g.4099375C>T	GRCh38
NC_000019.9:g.4099373C>T , CM000681.1:g.4099373C>T	GRCh37
NC_000019.8:g.4050373C>T	NCBI36
NG_007996.1:g.29754G>A , LRG_750:g.29754G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1184G>A
ENST00000687128.1:n.1184G>A
ENST00000688002.1:n.1039G>A
ENST00000689792.1:n.649G>A
ENST00000262948.10:c.745G>A MANE Select	ENSP00000262948.4:p.Asp249Asn
ENST00000262948.9:c.745G>A	ENSP00000262948.3:p.Asp249Asn
ENST00000394867.8:c.454G>A	ENSP00000378336.1:p.Asp152Asn
ENST00000593364.5:n.692G>A
ENST00000595715.1:n.560G>A
ENST00000597263.5:n.169+1644G>A
ENST00000599021.1:c.29+1644G>A
ENST00000600584.5:n.1305G>A
ENST00000601786.5:n.1046G>A
NM_030662.3:c.745G>A , LRG_750t1:c.745G>A	NP_109587.1:p.Asp249Asn
XM_006722799.2:c.705+1644G>A	XP_006722862.1:n.705+1644G>A
XM_011528133.1:c.175G>A	XP_011526435.1:p.Asp59Asn
XM_017026989.1:c.745G>A	XP_016882478.1:p.Asp249Asn
XM_017026990.1:c.705+1644G>A	XP_016882479.1:n.705+1644G>A
NM_030662.4:c.745G>A MANE Select	NP_109587.1:p.Asp249Asn