Canonical Allele Identifier: CA471156217

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.101997896T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100238139T>A , CM000672.2:g.100238139T>A	GRCh38
NC_000010.10:g.101997896T>A , CM000672.1:g.101997896T>A	GRCh37
NC_000010.9:g.101987886T>A	NCBI36
NG_041811.1:g.34543A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.1137A>T MANE Select	ENSP00000326411.6:p.Ala379=
ENST00000354105.8:c.1137A>T	ENSP00000326411.6:p.Ala379=
ENST00000370379.1:c.402A>T	ENSP00000359405.1:p.Ala134=
ENST00000468709.5:n.993A>T
ENST00000478047.1:n.1292A>T
ENST00000482452.5:n.820A>T
NM_001303404.1:c.1137A>T	NP_001290333.1:p.Ala379=
NM_001303405.1:c.726A>T	NP_001290334.1:p.Ala242=
NM_001303406.1:c.726A>T	NP_001290335.1:p.Ala242=
NM_001303407.1:c.402A>T	NP_001290336.1:p.Ala134=
NM_018294.5:c.1137A>T	NP_060764.3:p.Ala379=
NM_018294.6:c.1137A>T MANE Select	NP_060764.3:p.Ala379=
NM_001303404.2:c.1137A>T	NP_001290333.1:p.Ala379=
NM_001303405.2:c.726A>T	NP_001290334.1:p.Ala242=
NM_001303406.2:c.726A>T	NP_001290335.1:p.Ala242=
NM_001303407.2:c.402A>T	NP_001290336.1:p.Ala134=