Canonical Allele Identifier: CA378163863

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.102005577G>T (hg19) ; chr10:g.100245820G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245820G>T , CM000672.2:g.100245820G>T	GRCh38
NC_000010.10:g.102005577G>T , CM000672.1:g.102005577G>T	GRCh37
NC_000010.9:g.101995567G>T	NCBI36
NG_041811.1:g.26862C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.943C>A MANE Select	ENSP00000326411.6:p.Pro315Thr
ENST00000354105.8:c.943C>A	ENSP00000326411.6:p.Pro315Thr
ENST00000370379.1:c.208C>A	ENSP00000359405.1:p.Pro70Thr
ENST00000466408.1:n.297C>A
ENST00000466955.5:n.484C>A
ENST00000468709.5:n.799C>A
ENST00000478047.1:n.1200-7589C>A
ENST00000482452.5:n.631C>A
ENST00000496796.5:n.707C>A
NM_001303404.1:c.943C>A	NP_001290333.1:p.Pro315Thr
NM_001303405.1:c.532C>A	NP_001290334.1:p.Pro178Thr
NM_001303406.1:c.532C>A	NP_001290335.1:p.Pro178Thr
NM_001303407.1:c.208C>A	NP_001290336.1:p.Pro70Thr
NM_018294.5:c.943C>A	NP_060764.3:p.Pro315Thr
NM_018294.6:c.943C>A MANE Select	NP_060764.3:p.Pro315Thr
NM_001303404.2:c.943C>A	NP_001290333.1:p.Pro315Thr
NM_001303405.2:c.532C>A	NP_001290334.1:p.Pro178Thr
NM_001303406.2:c.532C>A	NP_001290335.1:p.Pro178Thr
NM_001303407.2:c.208C>A	NP_001290336.1:p.Pro70Thr