Canonical Allele Identifier: CA931782112

Gene: CWF19L1

Linked Data

• gnomAD v3: 10-100245797-ACGAGGTTTGCGAGGCTGCTTTGGATGAGGAGAAGATTTGCTATCTCTACCTGTGGATGAACGCTTCCTTCCCTG-A
• gnomAD v4: 10-100245797-ACGAGGTTTGCGAGGCTGCTTTGGATGAGGAGAAGATTTGCTATCTCTACCTGTGGATGAACGCTTCCTTCCCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245799_100245872del , CM000672.2:g.100245799_100245872del	GRCh38
NC_000010.10:g.102005556_102005629del , CM000672.1:g.102005556_102005629del	GRCh37
NC_000010.9:g.101995546_101995619del	NCBI36
NG_041811.1:g.26811_26884del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.892_964+1del
ENST00000354105.8:c.892_964+1del
ENST00000370379.1:c.157_229+1del
ENST00000466408.1:n.246_318+1del
ENST00000466955.5:n.433_505+1del
ENST00000468709.5:n.748_820+1del
ENST00000478047.1:n.1199+7550_1200-7567del
ENST00000482452.5:n.580_652+1del
NM_001303404.1:c.892_964+1del
NM_001303405.1:c.481_553+1del
NM_001303406.1:c.481_553+1del
NM_001303407.1:c.157_229+1del
NM_018294.5:c.892_964+1del
NM_018294.6:c.892_964+1del
NM_001303404.2:c.892_964+1del
NM_001303405.2:c.481_553+1del
NM_001303406.2:c.481_553+1del
NM_001303407.2:c.157_229+1del