Canonical Allele Identifier: CA1931677452

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100238140G= , CM000672.2:g.100238140G=	GRCh38
NC_000010.10:g.101997897G= , CM000672.1:g.101997897G=	GRCh37
NC_000010.9:g.101987887G=	NCBI36
NG_041811.1:g.34542C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.1136C= MANE Select	ENSP00000326411.6:p.Ala379=
ENST00000354105.8:c.1136C=	ENSP00000326411.6:p.Ala379=
ENST00000370379.1:c.401C=	ENSP00000359405.1:p.Ala134=
ENST00000468709.5:n.992C=
ENST00000478047.1:n.1291C=
ENST00000482452.5:n.819C=
NM_001303404.1:c.1136C=	NP_001290333.1:p.Ala379=
NM_001303405.1:c.725C=	NP_001290334.1:p.Ala242=
NM_001303406.1:c.725C=	NP_001290335.1:p.Ala242=
NM_001303407.1:c.401C=	NP_001290336.1:p.Ala134=
NM_018294.5:c.1136C=	NP_060764.3:p.Ala379=
NM_018294.6:c.1136C= MANE Select	NP_060764.3:p.Ala379=
NM_001303404.2:c.1136C=	NP_001290333.1:p.Ala379=
NM_001303405.2:c.725C=	NP_001290334.1:p.Ala242=
NM_001303406.2:c.725C=	NP_001290335.1:p.Ala242=
NM_001303407.2:c.401C=	NP_001290336.1:p.Ala134=