Canonical Allele Identifier: CA2517987381
Gene: CELF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.10560136_10560137insCTACAGA , CM000672.2:g.10560136_10560137insCTACAGA GRCh38
NC_000010.10:g.10602099_10602100insCTACAGA , CM000672.1:g.10602099_10602100insCTACAGA GRCh37
NC_000010.9:g.10642105_10642106insCTACAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001326317.1:c.-95+97550_-95+97551insCTACAGA NP_001313246.1:n.-95+97550_-95+97551insCTACAGA
NM_001326318.1:c.-95+97550_-95+97551insCTACAGA NP_001313247.1:n.-95+97550_-95+97551insCTACAGA
NM_001326319.1:c.-133+97550_-133+97551insCTACAGA NP_001313248.1:n.-133+97550_-133+97551insCTACAGA
NM_001326320.1:c.-189+97550_-189+97551insCTACAGA NP_001313249.1:n.-189+97550_-189+97551insCTACAGA
NM_001326321.1:c.-95+97550_-95+97551insCTACAGA NP_001313250.1:n.-95+97550_-95+97551insCTACAGA
NM_001326323.1:c.-189+97550_-189+97551insCTACAGA NP_001313252.1:n.-189+97550_-189+97551insCTACAGA
XM_017015557.1:c.-273+97550_-273+97551insCTACAGA XP_016871046.1:n.-273+97550_-273+97551insCTACAGA
XM_017015568.2:c.-627+97550_-627+97551insCTACAGA XP_016871057.1:n.-627+97550_-627+97551insCTACAGA
NM_001326317.2:c.-95+97550_-95+97551insCTACAGA NP_001313246.1:n.-95+97550_-95+97551insCTACAGA
NM_001326318.2:c.-95+97550_-95+97551insCTACAGA NP_001313247.1:n.-95+97550_-95+97551insCTACAGA
NM_001326319.2:c.-133+97550_-133+97551insCTACAGA NP_001313248.1:n.-133+97550_-133+97551insCTACAGA
NM_001326320.2:c.-189+97550_-189+97551insCTACAGA NP_001313249.1:n.-189+97550_-189+97551insCTACAGA
NM_001326321.2:c.-95+97550_-95+97551insCTACAGA NP_001313250.1:n.-95+97550_-95+97551insCTACAGA
NM_001326323.2:c.-189+97550_-189+97551insCTACAGA NP_001313252.1:n.-189+97550_-189+97551insCTACAGA