Canonical Allele Identifier: CA504984452
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4094484G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4094486G>A , CM000681.2:g.4094486G>A GRCh38
NC_000019.9:g.4094484G>A , CM000681.1:g.4094484G>A GRCh37
NC_000019.8:g.4045484G>A NCBI36
NG_007996.1:g.34643C>T , LRG_750:g.34643C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1498C>T
ENST00000688002.1:n.3210C>T
ENST00000688751.1:n.195C>T
ENST00000689792.1:n.963C>T
ENST00000262948.10:c.1059C>T MANE Select ENSP00000262948.4:p.Asn353=
ENST00000262948.9:c.1059C>T ENSP00000262948.3:p.Asn353=
ENST00000394867.8:c.768C>T ENSP00000378336.1:p.Asn256=
ENST00000597263.5:n.244C>T
ENST00000599021.1:c.169C>T
ENST00000600584.5:n.2508C>T
ENST00000601786.5:n.1360C>T
NM_030662.3:c.1059C>T , LRG_750t1:c.1059C>T NP_109587.1:p.Asn353=
XM_006722799.2:c.780C>T XP_006722862.1:p.Asn260=
XM_011528133.1:c.489C>T XP_011526435.1:p.Asn163=
NM_030662.4:c.1059C>T MANE Select NP_109587.1:p.Asn353=