Canonical Allele Identifier: CA2786619365

Gene: CELF2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.10560269T>A , CM000672.2:g.10560269T>A	GRCh38
NC_000010.10:g.10602232T>A , CM000672.1:g.10602232T>A	GRCh37
NC_000010.9:g.10642238T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001326317.1:c.-95+97683T>A	NP_001313246.1:n.-95+97683T>A
NM_001326318.1:c.-95+97683T>A	NP_001313247.1:n.-95+97683T>A
NM_001326319.1:c.-133+97683T>A	NP_001313248.1:n.-133+97683T>A
NM_001326320.1:c.-189+97683T>A	NP_001313249.1:n.-189+97683T>A
NM_001326321.1:c.-95+97683T>A	NP_001313250.1:n.-95+97683T>A
NM_001326323.1:c.-189+97683T>A	NP_001313252.1:n.-189+97683T>A
XM_017015557.1:c.-273+97683T>A	XP_016871046.1:n.-273+97683T>A
XM_017015568.2:c.-627+97683T>A	XP_016871057.1:n.-627+97683T>A
NM_001326317.2:c.-95+97683T>A	NP_001313246.1:n.-95+97683T>A
NM_001326318.2:c.-95+97683T>A	NP_001313247.1:n.-95+97683T>A
NM_001326319.2:c.-133+97683T>A	NP_001313248.1:n.-133+97683T>A
NM_001326320.2:c.-189+97683T>A	NP_001313249.1:n.-189+97683T>A
NM_001326321.2:c.-95+97683T>A	NP_001313250.1:n.-95+97683T>A
NM_001326323.2:c.-189+97683T>A	NP_001313252.1:n.-189+97683T>A