Canonical Allele Identifier: CA403383324

Gene: MAP2K2

Linked Data

• COSMIC: COSM3960073 ; COSM3960074
• MyVariant Identifiers: chr19:g.4095411C>G (hg19) ; chr19:g.4095413C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095413C>G , CM000681.2:g.4095413C>G	GRCh38
NC_000019.9:g.4095411C>G , CM000681.1:g.4095411C>G	GRCh37
NC_000019.8:g.4046411C>G	NCBI36
NG_007996.1:g.33716G>C , LRG_750:g.33716G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1460G>C
ENST00000688002.1:n.3172G>C
ENST00000688751.1:n.157G>C
ENST00000689792.1:n.925G>C
ENST00000262948.10:c.1021G>C MANE Select	ENSP00000262948.4:p.Asp341His
ENST00000262948.9:c.1021G>C	ENSP00000262948.3:p.Asp341His
ENST00000394867.8:c.730G>C	ENSP00000378336.1:p.Asp244His
ENST00000595715.1:n.836G>C
ENST00000597263.5:n.206G>C
ENST00000599021.1:c.131G>C
ENST00000600584.5:n.1581G>C
ENST00000601786.5:n.1322G>C
NM_030662.3:c.1021G>C , LRG_750t1:c.1021G>C	NP_109587.1:p.Asp341His
XM_006722799.2:c.742G>C	XP_006722862.1:p.Asp248His
XM_011528133.1:c.451G>C	XP_011526435.1:p.Asp151His
XM_017026989.1:c.1021G>C	XP_016882478.1:p.Asp341His
XM_017026990.1:c.742G>C	XP_016882479.1:p.Asp248His
NM_030662.4:c.1021G>C MANE Select	NP_109587.1:p.Asp341His