Canonical Allele Identifier: CA403383435

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4095437T>C (hg19) ; chr19:g.4095439T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095439T>C , CM000681.2:g.4095439T>C	GRCh38
NC_000019.9:g.4095437T>C , CM000681.1:g.4095437T>C	GRCh37
NC_000019.8:g.4046437T>C	NCBI36
NG_007996.1:g.33690A>G , LRG_750:g.33690A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1434A>G
ENST00000688002.1:n.3146A>G
ENST00000688751.1:n.131A>G
ENST00000689792.1:n.899A>G
ENST00000262948.10:c.995A>G MANE Select	ENSP00000262948.4:p.Lys332Arg
ENST00000262948.9:c.995A>G	ENSP00000262948.3:p.Lys332Arg
ENST00000394867.8:c.704A>G	ENSP00000378336.1:p.Lys235Arg
ENST00000595715.1:n.810A>G
ENST00000597263.5:n.180A>G
ENST00000599021.1:c.105A>G
ENST00000600584.5:n.1555A>G
ENST00000601786.5:n.1296A>G
NM_030662.3:c.995A>G , LRG_750t1:c.995A>G	NP_109587.1:p.Lys332Arg
XM_006722799.2:c.716A>G	XP_006722862.1:p.Lys239Arg
XM_011528133.1:c.425A>G	XP_011526435.1:p.Lys142Arg
XM_017026989.1:c.995A>G	XP_016882478.1:p.Lys332Arg
XM_017026990.1:c.716A>G	XP_016882479.1:p.Lys239Arg
NM_030662.4:c.995A>G MANE Select	NP_109587.1:p.Lys332Arg