Canonical Allele Identifier: CA2610520583

Gene: CWF19L1

Linked Data

• gnomAD v4: 10-100245929-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245929G>C , CM000672.2:g.100245929G>C	GRCh38
NC_000010.10:g.102005686G>C , CM000672.1:g.102005686G>C	GRCh37
NC_000010.9:g.101995676G>C	NCBI36
NG_041811.1:g.26753C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.850-16C>G MANE Select	ENSP00000326411.6:n.850-16C>G
ENST00000354105.8:c.850-16C>G	ENSP00000326411.6:n.850-16C>G
ENST00000370379.1:c.115-16C>G	ENSP00000359405.1:n.115-16C>G
ENST00000466408.1:n.188C>G
ENST00000466955.5:n.391-16C>G
ENST00000468709.5:n.706-16C>G
ENST00000478047.1:n.1199+7492C>G
ENST00000482452.5:n.538-16C>G
ENST00000496796.5:n.614-16C>G
NM_001303404.1:c.850-16C>G	NP_001290333.1:n.850-16C>G
NM_001303405.1:c.439-16C>G	NP_001290334.1:n.439-16C>G
NM_001303406.1:c.439-16C>G	NP_001290335.1:n.439-16C>G
NM_001303407.1:c.115-16C>G	NP_001290336.1:n.115-16C>G
NM_018294.5:c.850-16C>G	NP_060764.3:n.850-16C>G
NM_018294.6:c.850-16C>G MANE Select	NP_060764.3:n.850-16C>G
NM_001303404.2:c.850-16C>G	NP_001290333.1:n.850-16C>G
NM_001303405.2:c.439-16C>G	NP_001290334.1:n.439-16C>G
NM_001303406.2:c.439-16C>G	NP_001290335.1:n.439-16C>G
NM_001303407.2:c.115-16C>G	NP_001290336.1:n.115-16C>G