Canonical Allele Identifier: CA378157710

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.102013182A>T (hg19) ; chr10:g.100253425A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100253425A>T , CM000672.2:g.100253425A>T	GRCh38
NC_000010.10:g.102013182A>T , CM000672.1:g.102013182A>T	GRCh37
NC_000010.9:g.102003172A>T	NCBI36
NG_041811.1:g.19257T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.619T>A MANE Select	ENSP00000326411.6:p.Tyr207Asn
ENST00000354105.8:c.619T>A	ENSP00000326411.6:p.Tyr207Asn
ENST00000466955.5:n.176T>A
ENST00000468709.5:n.475T>A
ENST00000473842.1:n.591T>A
ENST00000478047.1:n.1195T>A
ENST00000482452.5:n.307T>A
ENST00000496796.5:n.383T>A
NM_001303404.1:c.619T>A	NP_001290333.1:p.Tyr207Asn
NM_001303405.1:c.208T>A	NP_001290334.1:p.Tyr70Asn
NM_001303406.1:c.208T>A	NP_001290335.1:p.Tyr70Asn
NM_001303407.1:c.-117T>A	NP_001290336.1:n.-117T>A
NM_018294.5:c.619T>A	NP_060764.3:p.Tyr207Asn
NM_018294.6:c.619T>A MANE Select	NP_060764.3:p.Tyr207Asn
NM_001303404.2:c.619T>A	NP_001290333.1:p.Tyr207Asn
NM_001303405.2:c.208T>A	NP_001290334.1:p.Tyr70Asn
NM_001303406.2:c.208T>A	NP_001290335.1:p.Tyr70Asn
NM_001303407.2:c.-117T>A	NP_001290336.1:n.-117T>A