Canonical Allele Identifier: CA378161857

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.101997901A>T (hg19) ; chr10:g.100238144A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100238144A>T , CM000672.2:g.100238144A>T	GRCh38
NC_000010.10:g.101997901A>T , CM000672.1:g.101997901A>T	GRCh37
NC_000010.9:g.101987891A>T	NCBI36
NG_041811.1:g.34538T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.1132T>A MANE Select	ENSP00000326411.6:p.Ser378Thr
ENST00000354105.8:c.1132T>A	ENSP00000326411.6:p.Ser378Thr
ENST00000370379.1:c.397T>A	ENSP00000359405.1:p.Ser133Thr
ENST00000468709.5:n.988T>A
ENST00000478047.1:n.1287T>A
ENST00000482452.5:n.815T>A
NM_001303404.1:c.1132T>A	NP_001290333.1:p.Ser378Thr
NM_001303405.1:c.721T>A	NP_001290334.1:p.Ser241Thr
NM_001303406.1:c.721T>A	NP_001290335.1:p.Ser241Thr
NM_001303407.1:c.397T>A	NP_001290336.1:p.Ser133Thr
NM_018294.5:c.1132T>A	NP_060764.3:p.Ser378Thr
NM_018294.6:c.1132T>A MANE Select	NP_060764.3:p.Ser378Thr
NM_001303404.2:c.1132T>A	NP_001290333.1:p.Ser378Thr
NM_001303405.2:c.721T>A	NP_001290334.1:p.Ser241Thr
NM_001303406.2:c.721T>A	NP_001290335.1:p.Ser241Thr
NM_001303407.2:c.397T>A	NP_001290336.1:p.Ser133Thr