Canonical Allele Identifier: CA403380895
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090645T>G (hg19) chr19:g.4090647T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090647T>G , CM000681.2:g.4090647T>G GRCh38
NC_000019.9:g.4090645T>G , CM000681.1:g.4090645T>G GRCh37
NC_000019.8:g.4041645T>G NCBI36
NG_007996.1:g.38482A>C , LRG_750:g.38482A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1593A>C
ENST00000688002.1:n.3305A>C
ENST00000688751.1:n.290A>C
ENST00000689792.1:n.1058A>C
ENST00000262948.10:c.1154A>C MANE Select ENSP00000262948.4:p.Lys385Thr
ENST00000262948.9:c.1154A>C ENSP00000262948.3:p.Lys385Thr
ENST00000394867.8:c.863A>C ENSP00000378336.1:p.Lys288Thr
ENST00000597263.5:n.339A>C
ENST00000599021.1:c.264A>C
ENST00000600584.5:n.2603A>C
ENST00000601786.5:n.1455A>C
NM_030662.3:c.1154A>C , LRG_750t1:c.1154A>C NP_109587.1:p.Lys385Thr
XM_006722799.2:c.875A>C XP_006722862.1:p.Lys292Thr
XM_011528133.1:c.584A>C XP_011526435.1:p.Lys195Thr
NM_030662.4:c.1154A>C MANE Select NP_109587.1:p.Lys385Thr
Search 100 bp 5'
Search 100 bp 3'