Canonical Allele Identifier: CA1931685896

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245752T= , CM000672.2:g.100245752T=	GRCh38
NC_000010.10:g.102005509T= , CM000672.1:g.102005509T=	GRCh37
NC_000010.9:g.101995499T=	NCBI36
NG_041811.1:g.26930A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.964+47A= MANE Select	ENSP00000326411.6:n.964+47A=
ENST00000354105.8:c.964+47A=	ENSP00000326411.6:n.964+47A=
ENST00000370379.1:c.229+47A=	ENSP00000359405.1:n.229+47A=
ENST00000466408.1:n.318+47A=
ENST00000466955.5:n.505+47A=
ENST00000468709.5:n.820+47A=
ENST00000478047.1:n.1200-7521A=
ENST00000482452.5:n.652+47A=
NM_001303404.1:c.964+47A=	NP_001290333.1:n.964+47A=
NM_001303405.1:c.553+47A=	NP_001290334.1:n.553+47A=
NM_001303406.1:c.553+47A=	NP_001290335.1:n.553+47A=
NM_001303407.1:c.229+47A=	NP_001290336.1:n.229+47A=
NM_018294.5:c.964+47A=	NP_060764.3:n.964+47A=
NM_018294.6:c.964+47A= MANE Select	NP_060764.3:n.964+47A=
NM_001303404.2:c.964+47A=	NP_001290333.1:n.964+47A=
NM_001303405.2:c.553+47A=	NP_001290334.1:n.553+47A=
NM_001303406.2:c.553+47A=	NP_001290335.1:n.553+47A=
NM_001303407.2:c.229+47A=	NP_001290336.1:n.229+47A=