Canonical Allele Identifier: CA403380871
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090643T>A (hg19) chr19:g.4090645T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090645T>A , CM000681.2:g.4090645T>A GRCh38
NC_000019.9:g.4090643T>A , CM000681.1:g.4090643T>A GRCh37
NC_000019.8:g.4041643T>A NCBI36
NG_007996.1:g.38484A>T , LRG_750:g.38484A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1595A>T
ENST00000688002.1:n.3307A>T
ENST00000688751.1:n.292A>T
ENST00000689792.1:n.1060A>T
ENST00000262948.10:c.1156A>T MANE Select ENSP00000262948.4:p.Thr386Ser
ENST00000262948.9:c.1156A>T ENSP00000262948.3:p.Thr386Ser
ENST00000394867.8:c.865A>T ENSP00000378336.1:p.Thr289Ser
ENST00000597263.5:n.341A>T
ENST00000599021.1:c.266A>T
ENST00000600584.5:n.2605A>T
ENST00000601786.5:n.1457A>T
NM_030662.3:c.1156A>T , LRG_750t1:c.1156A>T NP_109587.1:p.Thr386Ser
XM_006722799.2:c.877A>T XP_006722862.1:p.Thr293Ser
XM_011528133.1:c.586A>T XP_011526435.1:p.Thr196Ser
NM_030662.4:c.1156A>T MANE Select NP_109587.1:p.Thr386Ser
Search 100 bp 5'
Search 100 bp 3'