Canonical Allele Identifier: CA1890224704

Gene: CELF2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.10559934C= , CM000672.2:g.10559934C=	GRCh38
NC_000010.10:g.10601897C= , CM000672.1:g.10601897C=	GRCh37
NC_000010.9:g.10641903C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001326317.1:c.-95+97348C=	NP_001313246.1:n.-95+97348C=
NM_001326318.1:c.-95+97348C=	NP_001313247.1:n.-95+97348C=
NM_001326319.1:c.-133+97348C=	NP_001313248.1:n.-133+97348C=
NM_001326320.1:c.-189+97348C=	NP_001313249.1:n.-189+97348C=
NM_001326321.1:c.-95+97348C=	NP_001313250.1:n.-95+97348C=
NM_001326323.1:c.-189+97348C=	NP_001313252.1:n.-189+97348C=
XM_017015557.1:c.-273+97348C=	XP_016871046.1:n.-273+97348C=
XM_017015568.2:c.-627+97348C=	XP_016871057.1:n.-627+97348C=
NM_001326317.2:c.-95+97348C=	NP_001313246.1:n.-95+97348C=
NM_001326318.2:c.-95+97348C=	NP_001313247.1:n.-95+97348C=
NM_001326319.2:c.-133+97348C=	NP_001313248.1:n.-133+97348C=
NM_001326320.2:c.-189+97348C=	NP_001313249.1:n.-189+97348C=
NM_001326321.2:c.-95+97348C=	NP_001313250.1:n.-95+97348C=
NM_001326323.2:c.-189+97348C=	NP_001313252.1:n.-189+97348C=