Canonical Allele Identifier: CA471157820

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.102005575T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245818T>A , CM000672.2:g.100245818T>A	GRCh38
NC_000010.10:g.102005575T>A , CM000672.1:g.102005575T>A	GRCh37
NC_000010.9:g.101995565T>A	NCBI36
NG_041811.1:g.26864A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.945A>T MANE Select	ENSP00000326411.6:p.Pro315=
ENST00000354105.8:c.945A>T	ENSP00000326411.6:p.Pro315=
ENST00000370379.1:c.210A>T	ENSP00000359405.1:p.Pro70=
ENST00000466408.1:n.299A>T
ENST00000466955.5:n.486A>T
ENST00000468709.5:n.801A>T
ENST00000478047.1:n.1200-7587A>T
ENST00000482452.5:n.633A>T
ENST00000496796.5:n.709A>T
NM_001303404.1:c.945A>T	NP_001290333.1:p.Pro315=
NM_001303405.1:c.534A>T	NP_001290334.1:p.Pro178=
NM_001303406.1:c.534A>T	NP_001290335.1:p.Pro178=
NM_001303407.1:c.210A>T	NP_001290336.1:p.Pro70=
NM_018294.5:c.945A>T	NP_060764.3:p.Pro315=
NM_018294.6:c.945A>T MANE Select	NP_060764.3:p.Pro315=
NM_001303404.2:c.945A>T	NP_001290333.1:p.Pro315=
NM_001303405.2:c.534A>T	NP_001290334.1:p.Pro178=
NM_001303406.2:c.534A>T	NP_001290335.1:p.Pro178=
NM_001303407.2:c.210A>T	NP_001290336.1:p.Pro70=