Canonical Allele Identifier: CA471156211

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.101997887T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100238130T>C , CM000672.2:g.100238130T>C	GRCh38
NC_000010.10:g.101997887T>C , CM000672.1:g.101997887T>C	GRCh37
NC_000010.9:g.101987877T>C	NCBI36
NG_041811.1:g.34552A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.1146A>G MANE Select	ENSP00000326411.6:p.Val382=
ENST00000354105.8:c.1146A>G	ENSP00000326411.6:p.Val382=
ENST00000370379.1:c.411A>G	ENSP00000359405.1:p.Val137=
ENST00000468709.5:n.1002A>G
ENST00000478047.1:n.1301A>G
ENST00000482452.5:n.829A>G
NM_001303404.1:c.1146A>G	NP_001290333.1:p.Val382=
NM_001303405.1:c.735A>G	NP_001290334.1:p.Val245=
NM_001303406.1:c.735A>G	NP_001290335.1:p.Val245=
NM_001303407.1:c.411A>G	NP_001290336.1:p.Val137=
NM_018294.5:c.1146A>G	NP_060764.3:p.Val382=
NM_018294.6:c.1146A>G MANE Select	NP_060764.3:p.Val382=
NM_001303404.2:c.1146A>G	NP_001290333.1:p.Val382=
NM_001303405.2:c.735A>G	NP_001290334.1:p.Val245=
NM_001303406.2:c.735A>G	NP_001290335.1:p.Val245=
NM_001303407.2:c.411A>G	NP_001290336.1:p.Val137=