Canonical Allele Identifier: CA403383352

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4095417T>G (hg19) ; chr19:g.4095419T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095419T>G , CM000681.2:g.4095419T>G	GRCh38
NC_000019.9:g.4095417T>G , CM000681.1:g.4095417T>G	GRCh37
NC_000019.8:g.4046417T>G	NCBI36
NG_007996.1:g.33710A>C , LRG_750:g.33710A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1454A>C
ENST00000688002.1:n.3166A>C
ENST00000688751.1:n.151A>C
ENST00000689792.1:n.919A>C
ENST00000262948.10:c.1015A>C MANE Select	ENSP00000262948.4:p.Thr339Pro
ENST00000262948.9:c.1015A>C	ENSP00000262948.3:p.Thr339Pro
ENST00000394867.8:c.724A>C	ENSP00000378336.1:p.Thr242Pro
ENST00000595715.1:n.830A>C
ENST00000597263.5:n.200A>C
ENST00000599021.1:c.125A>C
ENST00000600584.5:n.1575A>C
ENST00000601786.5:n.1316A>C
NM_030662.3:c.1015A>C , LRG_750t1:c.1015A>C	NP_109587.1:p.Thr339Pro
XM_006722799.2:c.736A>C	XP_006722862.1:p.Thr246Pro
XM_011528133.1:c.445A>C	XP_011526435.1:p.Thr149Pro
XM_017026989.1:c.1015A>C	XP_016882478.1:p.Thr339Pro
XM_017026990.1:c.736A>C	XP_016882479.1:p.Thr246Pro
NM_030662.4:c.1015A>C MANE Select	NP_109587.1:p.Thr339Pro