Canonical Allele Identifier: CA403380678
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090613T>A (hg19) chr19:g.4090615T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090615T>A , CM000681.2:g.4090615T>A GRCh38
NC_000019.9:g.4090613T>A , CM000681.1:g.4090613T>A GRCh37
NC_000019.8:g.4041613T>A NCBI36
NG_007996.1:g.38514A>T , LRG_750:g.38514A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1625A>T
ENST00000688002.1:n.3337A>T
ENST00000688751.1:n.322A>T
ENST00000689792.1:n.1090A>T
ENST00000262948.10:c.1186A>T MANE Select ENSP00000262948.4:p.Thr396Ser
ENST00000262948.9:c.1186A>T ENSP00000262948.3:p.Thr396Ser
ENST00000394867.8:c.895A>T ENSP00000378336.1:p.Thr299Ser
ENST00000597263.5:n.371A>T
ENST00000599021.1:c.296A>T
ENST00000600584.5:n.2635A>T
ENST00000601786.5:n.1487A>T
NM_030662.3:c.1186A>T , LRG_750t1:c.1186A>T NP_109587.1:p.Thr396Ser
XM_006722799.2:c.907A>T XP_006722862.1:p.Thr303Ser
XM_011528133.1:c.616A>T XP_011526435.1:p.Thr206Ser
NM_030662.4:c.1186A>T MANE Select NP_109587.1:p.Thr396Ser
Search 100 bp 5'
Search 100 bp 3'