Canonical Allele Identifier: CA378161790

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.101997891A>C (hg19) ; chr10:g.100238134A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100238134A>C , CM000672.2:g.100238134A>C	GRCh38
NC_000010.10:g.101997891A>C , CM000672.1:g.101997891A>C	GRCh37
NC_000010.9:g.101987881A>C	NCBI36
NG_041811.1:g.34548T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.1142T>G MANE Select	ENSP00000326411.6:p.Val381Gly
ENST00000354105.8:c.1142T>G	ENSP00000326411.6:p.Val381Gly
ENST00000370379.1:c.407T>G	ENSP00000359405.1:p.Val136Gly
ENST00000468709.5:n.998T>G
ENST00000478047.1:n.1297T>G
ENST00000482452.5:n.825T>G
NM_001303404.1:c.1142T>G	NP_001290333.1:p.Val381Gly
NM_001303405.1:c.731T>G	NP_001290334.1:p.Val244Gly
NM_001303406.1:c.731T>G	NP_001290335.1:p.Val244Gly
NM_001303407.1:c.407T>G	NP_001290336.1:p.Val136Gly
NM_018294.5:c.1142T>G	NP_060764.3:p.Val381Gly
NM_018294.6:c.1142T>G MANE Select	NP_060764.3:p.Val381Gly
NM_001303404.2:c.1142T>G	NP_001290333.1:p.Val381Gly
NM_001303405.2:c.731T>G	NP_001290334.1:p.Val244Gly
NM_001303406.2:c.731T>G	NP_001290335.1:p.Val244Gly
NM_001303407.2:c.407T>G	NP_001290336.1:p.Val136Gly