Canonical Allele Identifier: CA1931696646

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100253422G= , CM000672.2:g.100253422G=	GRCh38
NC_000010.10:g.102013179G= , CM000672.1:g.102013179G=	GRCh37
NC_000010.9:g.102003169G=	NCBI36
NG_041811.1:g.19260C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.622C= MANE Select	ENSP00000326411.6:p.Arg208=
ENST00000354105.8:c.622C=	ENSP00000326411.6:p.Arg208=
ENST00000466955.5:n.179C=
ENST00000468709.5:n.478C=
ENST00000473842.1:n.594C=
ENST00000478047.1:n.1198C=
ENST00000482452.5:n.310C=
ENST00000496796.5:n.386C=
NM_001303404.1:c.622C=	NP_001290333.1:p.Arg208=
NM_001303405.1:c.211C=	NP_001290334.1:p.Arg71=
NM_001303406.1:c.211C=	NP_001290335.1:p.Arg71=
NM_001303407.1:c.-114C=	NP_001290336.1:n.-114C=
NM_018294.5:c.622C=	NP_060764.3:p.Arg208=
NM_018294.6:c.622C= MANE Select	NP_060764.3:p.Arg208=
NM_001303404.2:c.622C=	NP_001290333.1:p.Arg208=
NM_001303405.2:c.211C=	NP_001290334.1:p.Arg71=
NM_001303406.2:c.211C=	NP_001290335.1:p.Arg71=
NM_001303407.2:c.-114C=	NP_001290336.1:n.-114C=