Canonical Allele Identifier: CA378161836

Gene: CWF19L1

Linked Data

• dbSNP Id: rs762678900
• MyVariant Identifiers: chr10:g.101997897G>A (hg19) ; chr10:g.100238140G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100238140G>A , CM000672.2:g.100238140G>A	GRCh38
NC_000010.10:g.101997897G>A , CM000672.1:g.101997897G>A	GRCh37
NC_000010.9:g.101987887G>A	NCBI36
NG_041811.1:g.34542C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.1136C>T MANE Select	ENSP00000326411.6:p.Ala379Val
ENST00000354105.8:c.1136C>T	ENSP00000326411.6:p.Ala379Val
ENST00000370379.1:c.401C>T	ENSP00000359405.1:p.Ala134Val
ENST00000468709.5:n.992C>T
ENST00000478047.1:n.1291C>T
ENST00000482452.5:n.819C>T
NM_001303404.1:c.1136C>T	NP_001290333.1:p.Ala379Val
NM_001303405.1:c.725C>T	NP_001290334.1:p.Ala242Val
NM_001303406.1:c.725C>T	NP_001290335.1:p.Ala242Val
NM_001303407.1:c.401C>T	NP_001290336.1:p.Ala134Val
NM_018294.5:c.1136C>T	NP_060764.3:p.Ala379Val
NM_018294.6:c.1136C>T MANE Select	NP_060764.3:p.Ala379Val
NM_001303404.2:c.1136C>T	NP_001290333.1:p.Ala379Val
NM_001303405.2:c.725C>T	NP_001290334.1:p.Ala242Val
NM_001303406.2:c.725C>T	NP_001290335.1:p.Ala242Val
NM_001303407.2:c.401C>T	NP_001290336.1:p.Ala134Val