Canonical Allele Identifier: CA304449271

Gene: MAP2K2

Linked Data

• dbSNP Id: rs371810699
• COSMIC: COSM5741357 ; COSM5741358
• MyVariant Identifiers: chr19:g.4099288G>A (hg19) ; chr19:g.4099290G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099290G>A , CM000681.2:g.4099290G>A	GRCh38
NC_000019.9:g.4099288G>A , CM000681.1:g.4099288G>A	GRCh37
NC_000019.8:g.4050288G>A	NCBI36
NG_007996.1:g.29839C>T , LRG_750:g.29839C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1269C>T
ENST00000687128.1:n.1269C>T
ENST00000688002.1:n.1124C>T
ENST00000689792.1:n.734C>T
ENST00000262948.10:c.830C>T MANE Select	ENSP00000262948.4:p.Ala277Val
ENST00000262948.9:c.830C>T	ENSP00000262948.3:p.Ala277Val
ENST00000394867.8:c.539C>T	ENSP00000378336.1:p.Ala180Val
ENST00000593364.5:n.777C>T
ENST00000595715.1:n.645C>T
ENST00000597263.5:n.169+1729C>T
ENST00000599021.1:c.29+1729C>T
ENST00000600584.5:n.1390C>T
ENST00000601786.5:n.1131C>T
NM_030662.3:c.830C>T , LRG_750t1:c.830C>T	NP_109587.1:p.Ala277Val
XM_006722799.2:c.705+1729C>T	XP_006722862.1:n.705+1729C>T
XM_011528133.1:c.260C>T	XP_011526435.1:p.Ala87Val
XM_017026989.1:c.830C>T	XP_016882478.1:p.Ala277Val
XM_017026990.1:c.705+1729C>T	XP_016882479.1:n.705+1729C>T
NM_030662.4:c.830C>T MANE Select	NP_109587.1:p.Ala277Val