Canonical Allele Identifier: CA504984706

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4095439A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095441A>T , CM000681.2:g.4095441A>T	GRCh38
NC_000019.9:g.4095439A>T , CM000681.1:g.4095439A>T	GRCh37
NC_000019.8:g.4046439A>T	NCBI36
NG_007996.1:g.33688T>A , LRG_750:g.33688T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1432T>A
ENST00000688002.1:n.3144T>A
ENST00000688751.1:n.129T>A
ENST00000689792.1:n.897T>A
ENST00000262948.10:c.993T>A MANE Select	ENSP00000262948.4:p.Pro331=
ENST00000262948.9:c.993T>A	ENSP00000262948.3:p.Pro331=
ENST00000394867.8:c.702T>A	ENSP00000378336.1:p.Pro234=
ENST00000595715.1:n.808T>A
ENST00000597263.5:n.178T>A
ENST00000599021.1:c.103T>A
ENST00000600584.5:n.1553T>A
ENST00000601786.5:n.1294T>A
NM_030662.3:c.993T>A , LRG_750t1:c.993T>A	NP_109587.1:p.Pro331=
XM_006722799.2:c.714T>A	XP_006722862.1:p.Pro238=
XM_011528133.1:c.423T>A	XP_011526435.1:p.Pro141=
XM_017026989.1:c.993T>A	XP_016882478.1:p.Pro331=
XM_017026990.1:c.714T>A	XP_016882479.1:p.Pro238=
NM_030662.4:c.993T>A MANE Select	NP_109587.1:p.Pro331=