Canonical Allele Identifier: CA378163870

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.102005580G>T (hg19) ; chr10:g.100245823G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245823G>T , CM000672.2:g.100245823G>T	GRCh38
NC_000010.10:g.102005580G>T , CM000672.1:g.102005580G>T	GRCh37
NC_000010.9:g.101995570G>T	NCBI36
NG_041811.1:g.26859C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.940C>A MANE Select	ENSP00000326411.6:p.His314Asn
ENST00000354105.8:c.940C>A	ENSP00000326411.6:p.His314Asn
ENST00000370379.1:c.205C>A	ENSP00000359405.1:p.His69Asn
ENST00000466408.1:n.294C>A
ENST00000466955.5:n.481C>A
ENST00000468709.5:n.796C>A
ENST00000478047.1:n.1200-7592C>A
ENST00000482452.5:n.628C>A
ENST00000496796.5:n.704C>A
NM_001303404.1:c.940C>A	NP_001290333.1:p.His314Asn
NM_001303405.1:c.529C>A	NP_001290334.1:p.His177Asn
NM_001303406.1:c.529C>A	NP_001290335.1:p.His177Asn
NM_001303407.1:c.205C>A	NP_001290336.1:p.His69Asn
NM_018294.5:c.940C>A	NP_060764.3:p.His314Asn
NM_018294.6:c.940C>A MANE Select	NP_060764.3:p.His314Asn
NM_001303404.2:c.940C>A	NP_001290333.1:p.His314Asn
NM_001303405.2:c.529C>A	NP_001290334.1:p.His177Asn
NM_001303406.2:c.529C>A	NP_001290335.1:p.His177Asn
NM_001303407.2:c.205C>A	NP_001290336.1:p.His69Asn