Canonical Allele Identifier: CA2397004764
Gene: MAPK1 HGNC NCBI

Linked Data

dbSNP Id: rs11913721

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21855846A>T , CM000684.2:g.21855846A>T GRCh38
NC_000022.10:g.22210135A>T , CM000684.1:g.22210135A>T GRCh37
NC_000022.9:g.20540135A>T NCBI36
NG_023054.2:g.16835T>A , LRG_786:g.16835T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000215832.11:c.119+11476T>A MANE Select ENSP00000215832.7:n.119+11476T>A
ENST00000215832.10:c.119+11476T>A ENSP00000215832.6:n.119+11476T>A
ENST00000398822.7:c.119+11476T>A ENSP00000381803.3:n.119+11476T>A
ENST00000544786.1:c.119+11476T>A ENSP00000440842.1:n.119+11476T>A
NM_002745.4:c.119+11476T>A , LRG_786t1:c.119+11476T>A NP_002736.3:n.119+11476T>A
NM_138957.3:c.119+11476T>A , LRG_786t2:c.119+11476T>A NP_620407.1:n.119+11476T>A
NM_002745.5:c.119+11476T>A MANE Select NP_002736.3:n.119+11476T>A