Canonical Allele Identifier: CA403382415

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4094452G>C (hg19) ; chr19:g.4094454G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094454G>C , CM000681.2:g.4094454G>C	GRCh38
NC_000019.9:g.4094452G>C , CM000681.1:g.4094452G>C	GRCh37
NC_000019.8:g.4045452G>C	NCBI36
NG_007996.1:g.34675C>G , LRG_750:g.34675C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1530C>G
ENST00000688002.1:n.3242C>G
ENST00000688751.1:n.227C>G
ENST00000689792.1:n.995C>G
ENST00000262948.10:c.1091C>G MANE Select	ENSP00000262948.4:p.Thr364Arg
ENST00000262948.9:c.1091C>G	ENSP00000262948.3:p.Thr364Arg
ENST00000394867.8:c.800C>G	ENSP00000378336.1:p.Thr267Arg
ENST00000597263.5:n.276C>G
ENST00000599021.1:c.201C>G
ENST00000600584.5:n.2540C>G
ENST00000601786.5:n.1392C>G
NM_030662.3:c.1091C>G , LRG_750t1:c.1091C>G	NP_109587.1:p.Thr364Arg
XM_006722799.2:c.812C>G	XP_006722862.1:p.Thr271Arg
XM_011528133.1:c.521C>G	XP_011526435.1:p.Thr174Arg
NM_030662.4:c.1091C>G MANE Select	NP_109587.1:p.Thr364Arg