Canonical Allele Identifier: CA403380764
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090627T>A (hg19) chr19:g.4090629T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090629T>A , CM000681.2:g.4090629T>A GRCh38
NC_000019.9:g.4090627T>A , CM000681.1:g.4090627T>A GRCh37
NC_000019.8:g.4041627T>A NCBI36
NG_007996.1:g.38500A>T , LRG_750:g.38500A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1611A>T
ENST00000688002.1:n.3323A>T
ENST00000688751.1:n.308A>T
ENST00000689792.1:n.1076A>T
ENST00000262948.10:c.1172A>T MANE Select ENSP00000262948.4:p.Gln391Leu
ENST00000262948.9:c.1172A>T ENSP00000262948.3:p.Gln391Leu
ENST00000394867.8:c.881A>T ENSP00000378336.1:p.Gln294Leu
ENST00000597263.5:n.357A>T
ENST00000599021.1:c.282A>T
ENST00000600584.5:n.2621A>T
ENST00000601786.5:n.1473A>T
NM_030662.3:c.1172A>T , LRG_750t1:c.1172A>T NP_109587.1:p.Gln391Leu
XM_006722799.2:c.893A>T XP_006722862.1:p.Gln298Leu
XM_011528133.1:c.602A>T XP_011526435.1:p.Gln201Leu
NM_030662.4:c.1172A>T MANE Select NP_109587.1:p.Gln391Leu
Search 100 bp 5'
Search 100 bp 3'