Canonical Allele Identifier: CA1931686492

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245939A= , CM000672.2:g.100245939A=	GRCh38
NC_000010.10:g.102005696A= , CM000672.1:g.102005696A=	GRCh37
NC_000010.9:g.101995686A=	NCBI36
NG_041811.1:g.26743T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.850-26T= MANE Select	ENSP00000326411.6:n.850-26T=
ENST00000354105.8:c.850-26T=	ENSP00000326411.6:n.850-26T=
ENST00000370379.1:c.115-26T=	ENSP00000359405.1:n.115-26T=
ENST00000466408.1:n.178T=
ENST00000466955.5:n.391-26T=
ENST00000468709.5:n.706-26T=
ENST00000478047.1:n.1199+7482T=
ENST00000482452.5:n.538-26T=
ENST00000496796.5:n.614-26T=
NM_001303404.1:c.850-26T=	NP_001290333.1:n.850-26T=
NM_001303405.1:c.439-26T=	NP_001290334.1:n.439-26T=
NM_001303406.1:c.439-26T=	NP_001290335.1:n.439-26T=
NM_001303407.1:c.115-26T=	NP_001290336.1:n.115-26T=
NM_018294.5:c.850-26T=	NP_060764.3:n.850-26T=
NM_018294.6:c.850-26T= MANE Select	NP_060764.3:n.850-26T=
NM_001303404.2:c.850-26T=	NP_001290333.1:n.850-26T=
NM_001303405.2:c.439-26T=	NP_001290334.1:n.439-26T=
NM_001303406.2:c.439-26T=	NP_001290335.1:n.439-26T=
NM_001303407.2:c.115-26T=	NP_001290336.1:n.115-26T=