Canonical Allele Identifier: CA2540367196

Gene: CELF2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.10560088_10560089insC , CM000672.2:g.10560088_10560089insC	GRCh38
NC_000010.10:g.10602051_10602052insC , CM000672.1:g.10602051_10602052insC	GRCh37
NC_000010.9:g.10642057_10642058insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001326317.1:c.-95+97502_-95+97503insC	NP_001313246.1:n.-95+97502_-95+97503insC
NM_001326318.1:c.-95+97502_-95+97503insC	NP_001313247.1:n.-95+97502_-95+97503insC
NM_001326319.1:c.-133+97502_-133+97503insC	NP_001313248.1:n.-133+97502_-133+97503insC
NM_001326320.1:c.-189+97502_-189+97503insC	NP_001313249.1:n.-189+97502_-189+97503insC
NM_001326321.1:c.-95+97502_-95+97503insC	NP_001313250.1:n.-95+97502_-95+97503insC
NM_001326323.1:c.-189+97502_-189+97503insC	NP_001313252.1:n.-189+97502_-189+97503insC
XM_017015557.1:c.-273+97502_-273+97503insC	XP_016871046.1:n.-273+97502_-273+97503insC
XM_017015568.2:c.-627+97502_-627+97503insC	XP_016871057.1:n.-627+97502_-627+97503insC
NM_001326317.2:c.-95+97502_-95+97503insC	NP_001313246.1:n.-95+97502_-95+97503insC
NM_001326318.2:c.-95+97502_-95+97503insC	NP_001313247.1:n.-95+97502_-95+97503insC
NM_001326319.2:c.-133+97502_-133+97503insC	NP_001313248.1:n.-133+97502_-133+97503insC
NM_001326320.2:c.-189+97502_-189+97503insC	NP_001313249.1:n.-189+97502_-189+97503insC
NM_001326321.2:c.-95+97502_-95+97503insC	NP_001313250.1:n.-95+97502_-95+97503insC
NM_001326323.2:c.-189+97502_-189+97503insC	NP_001313252.1:n.-189+97502_-189+97503insC