Canonical Allele Identifier: CA1931686250

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245802G= , CM000672.2:g.100245802G=	GRCh38
NC_000010.10:g.102005559G= , CM000672.1:g.102005559G=	GRCh37
NC_000010.9:g.101995549G=	NCBI36
NG_041811.1:g.26880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.961C= MANE Select	ENSP00000326411.6:p.Pro321=
ENST00000354105.8:c.961C=	ENSP00000326411.6:p.Pro321=
ENST00000370379.1:c.226C=	ENSP00000359405.1:p.Pro76=
ENST00000466408.1:n.315C=
ENST00000466955.5:n.502C=
ENST00000468709.5:n.817C=
ENST00000478047.1:n.1200-7571C=
ENST00000482452.5:n.649C=
ENST00000496796.5:n.725C=
NM_001303404.1:c.961C=	NP_001290333.1:p.Pro321=
NM_001303405.1:c.550C=	NP_001290334.1:p.Pro184=
NM_001303406.1:c.550C=	NP_001290335.1:p.Pro184=
NM_001303407.1:c.226C=	NP_001290336.1:p.Pro76=
NM_018294.5:c.961C=	NP_060764.3:p.Pro321=
NM_018294.6:c.961C= MANE Select	NP_060764.3:p.Pro321=
NM_001303404.2:c.961C=	NP_001290333.1:p.Pro321=
NM_001303405.2:c.550C=	NP_001290334.1:p.Pro184=
NM_001303406.2:c.550C=	NP_001290335.1:p.Pro184=
NM_001303407.2:c.226C=	NP_001290336.1:p.Pro76=