Canonical Allele Identifier: CA403392712
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs2145080471

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4117546G>T , CM000681.2:g.4117546G>T GRCh38
NC_000019.9:g.4117544G>T , CM000681.1:g.4117544G>T GRCh37
NC_000019.8:g.4068544G>T NCBI36
NG_007996.1:g.11583C>A , LRG_750:g.11583C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394867.9:n.615C>A
ENST00000687128.1:n.615C>A
ENST00000262948.10:c.176C>A MANE Select ENSP00000262948.4:p.Thr59Asn
ENST00000262948.9:c.176C>A ENSP00000262948.3:p.Thr59Asn
ENST00000394867.8:c.-116C>A ENSP00000378336.1:n.-116C>A
ENST00000599345.1:n.373C>A
NM_030662.3:c.176C>A , LRG_750t1:c.176C>A NP_109587.1:p.Thr59Asn
XM_006722799.2:c.176C>A XP_006722862.1:p.Thr59Asn
XM_017026989.1:c.176C>A XP_016882478.1:p.Thr59Asn
XM_017026990.1:c.176C>A XP_016882479.1:p.Thr59Asn
XM_017026991.1:c.176C>A XP_016882480.1:p.Thr59Asn
NM_030662.4:c.176C>A MANE Select NP_109587.1:p.Thr59Asn