Canonical Allele Identifier: CA471157857

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.102005581A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245824A>T , CM000672.2:g.100245824A>T	GRCh38
NC_000010.10:g.102005581A>T , CM000672.1:g.102005581A>T	GRCh37
NC_000010.9:g.101995571A>T	NCBI36
NG_041811.1:g.26858T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.939T>A MANE Select	ENSP00000326411.6:p.Pro313=
ENST00000354105.8:c.939T>A	ENSP00000326411.6:p.Pro313=
ENST00000370379.1:c.204T>A	ENSP00000359405.1:p.Pro68=
ENST00000466408.1:n.293T>A
ENST00000466955.5:n.480T>A
ENST00000468709.5:n.795T>A
ENST00000478047.1:n.1200-7593T>A
ENST00000482452.5:n.627T>A
ENST00000496796.5:n.703T>A
NM_001303404.1:c.939T>A	NP_001290333.1:p.Pro313=
NM_001303405.1:c.528T>A	NP_001290334.1:p.Pro176=
NM_001303406.1:c.528T>A	NP_001290335.1:p.Pro176=
NM_001303407.1:c.204T>A	NP_001290336.1:p.Pro68=
NM_018294.5:c.939T>A	NP_060764.3:p.Pro313=
NM_018294.6:c.939T>A MANE Select	NP_060764.3:p.Pro313=
NM_001303404.2:c.939T>A	NP_001290333.1:p.Pro313=
NM_001303405.2:c.528T>A	NP_001290334.1:p.Pro176=
NM_001303406.2:c.528T>A	NP_001290335.1:p.Pro176=
NM_001303407.2:c.204T>A	NP_001290336.1:p.Pro68=