Canonical Allele Identifier: CA1931686264

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245808G= , CM000672.2:g.100245808G=	GRCh38
NC_000010.10:g.102005565G= , CM000672.1:g.102005565G=	GRCh37
NC_000010.9:g.101995555G=	NCBI36
NG_041811.1:g.26874C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.955C= MANE Select	ENSP00000326411.6:p.Arg319=
ENST00000354105.8:c.955C=	ENSP00000326411.6:p.Arg319=
ENST00000370379.1:c.220C=	ENSP00000359405.1:p.Arg74=
ENST00000466408.1:n.309C=
ENST00000466955.5:n.496C=
ENST00000468709.5:n.811C=
ENST00000478047.1:n.1200-7577C=
ENST00000482452.5:n.643C=
ENST00000496796.5:n.719C=
NM_001303404.1:c.955C=	NP_001290333.1:p.Arg319=
NM_001303405.1:c.544C=	NP_001290334.1:p.Arg182=
NM_001303406.1:c.544C=	NP_001290335.1:p.Arg182=
NM_001303407.1:c.220C=	NP_001290336.1:p.Arg74=
NM_018294.5:c.955C=	NP_060764.3:p.Arg319=
NM_018294.6:c.955C= MANE Select	NP_060764.3:p.Arg319=
NM_001303404.2:c.955C=	NP_001290333.1:p.Arg319=
NM_001303405.2:c.544C=	NP_001290334.1:p.Arg182=
NM_001303406.2:c.544C=	NP_001290335.1:p.Arg182=
NM_001303407.2:c.220C=	NP_001290336.1:p.Arg74=