Canonical Allele Identifier: CA1931686279

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245817T= , CM000672.2:g.100245817T=	GRCh38
NC_000010.10:g.102005574T= , CM000672.1:g.102005574T=	GRCh37
NC_000010.9:g.101995564T=	NCBI36
NG_041811.1:g.26865A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.946A= MANE Select	ENSP00000326411.6:p.Lys316=
ENST00000354105.8:c.946A=	ENSP00000326411.6:p.Lys316=
ENST00000370379.1:c.211A=	ENSP00000359405.1:p.Lys71=
ENST00000466408.1:n.300A=
ENST00000466955.5:n.487A=
ENST00000468709.5:n.802A=
ENST00000478047.1:n.1200-7586A=
ENST00000482452.5:n.634A=
ENST00000496796.5:n.710A=
NM_001303404.1:c.946A=	NP_001290333.1:p.Lys316=
NM_001303405.1:c.535A=	NP_001290334.1:p.Lys179=
NM_001303406.1:c.535A=	NP_001290335.1:p.Lys179=
NM_001303407.1:c.211A=	NP_001290336.1:p.Lys71=
NM_018294.5:c.946A=	NP_060764.3:p.Lys316=
NM_018294.6:c.946A= MANE Select	NP_060764.3:p.Lys316=
NM_001303404.2:c.946A=	NP_001290333.1:p.Lys316=
NM_001303405.2:c.535A=	NP_001290334.1:p.Lys179=
NM_001303406.2:c.535A=	NP_001290335.1:p.Lys179=
NM_001303407.2:c.211A=	NP_001290336.1:p.Lys71=