Canonical Allele Identifier: CA504984305
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090617T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090619T>A , CM000681.2:g.4090619T>A GRCh38
NC_000019.9:g.4090617T>A , CM000681.1:g.4090617T>A GRCh37
NC_000019.8:g.4041617T>A NCBI36
NG_007996.1:g.38510A>T , LRG_750:g.38510A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1621A>T
ENST00000688002.1:n.3333A>T
ENST00000688751.1:n.318A>T
ENST00000689792.1:n.1086A>T
ENST00000262948.10:c.1182A>T MANE Select ENSP00000262948.4:p.Thr394=
ENST00000262948.9:c.1182A>T ENSP00000262948.3:p.Thr394=
ENST00000394867.8:c.891A>T ENSP00000378336.1:p.Thr297=
ENST00000597263.5:n.367A>T
ENST00000599021.1:c.292A>T
ENST00000600584.5:n.2631A>T
ENST00000601786.5:n.1483A>T
NM_030662.3:c.1182A>T , LRG_750t1:c.1182A>T NP_109587.1:p.Thr394=
XM_006722799.2:c.903A>T XP_006722862.1:p.Thr301=
XM_011528133.1:c.612A>T XP_011526435.1:p.Thr204=
NM_030662.4:c.1182A>T MANE Select NP_109587.1:p.Thr394=