Canonical Allele Identifier: CA403383180

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145043476
• MyVariant Identifiers: chr19:g.4095395A>T (hg19) ; chr19:g.4095397A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095397A>T , CM000681.2:g.4095397A>T	GRCh38
NC_000019.9:g.4095395A>T , CM000681.1:g.4095395A>T	GRCh37
NC_000019.8:g.4046395A>T	NCBI36
NG_007996.1:g.33732T>A , LRG_750:g.33732T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1476T>A
ENST00000688002.1:n.3188T>A
ENST00000688751.1:n.173T>A
ENST00000689792.1:n.941T>A
ENST00000262948.10:c.1037T>A MANE Select	ENSP00000262948.4:p.Val346Asp
ENST00000262948.9:c.1037T>A	ENSP00000262948.3:p.Val346Asp
ENST00000394867.8:c.746T>A	ENSP00000378336.1:p.Val249Asp
ENST00000595715.1:n.852T>A
ENST00000597263.5:n.222T>A
ENST00000599021.1:c.147T>A
ENST00000600584.5:n.1597T>A
ENST00000601786.5:n.1338T>A
NM_030662.3:c.1037T>A , LRG_750t1:c.1037T>A	NP_109587.1:p.Val346Asp
XM_006722799.2:c.758T>A	XP_006722862.1:p.Val253Asp
XM_011528133.1:c.467T>A	XP_011526435.1:p.Val156Asp
XM_017026989.1:c.1037T>A	XP_016882478.1:p.Val346Asp
XM_017026990.1:c.758T>A	XP_016882479.1:p.Val253Asp
NM_030662.4:c.1037T>A MANE Select	NP_109587.1:p.Val346Asp