Canonical Allele Identifier: CA2610520581

Gene: CWF19L1

Linked Data

• gnomAD v4: 10-100245922-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245922G>A , CM000672.2:g.100245922G>A	GRCh38
NC_000010.10:g.102005679G>A , CM000672.1:g.102005679G>A	GRCh37
NC_000010.9:g.101995669G>A	NCBI36
NG_041811.1:g.26760C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.850-9C>T MANE Select	ENSP00000326411.6:n.850-9C>T
ENST00000354105.8:c.850-9C>T	ENSP00000326411.6:n.850-9C>T
ENST00000370379.1:c.115-9C>T	ENSP00000359405.1:n.115-9C>T
ENST00000466408.1:n.195C>T
ENST00000466955.5:n.391-9C>T
ENST00000468709.5:n.706-9C>T
ENST00000478047.1:n.1199+7499C>T
ENST00000482452.5:n.538-9C>T
ENST00000496796.5:n.614-9C>T
NM_001303404.1:c.850-9C>T	NP_001290333.1:n.850-9C>T
NM_001303405.1:c.439-9C>T	NP_001290334.1:n.439-9C>T
NM_001303406.1:c.439-9C>T	NP_001290335.1:n.439-9C>T
NM_001303407.1:c.115-9C>T	NP_001290336.1:n.115-9C>T
NM_018294.5:c.850-9C>T	NP_060764.3:n.850-9C>T
NM_018294.6:c.850-9C>T MANE Select	NP_060764.3:n.850-9C>T
NM_001303404.2:c.850-9C>T	NP_001290333.1:n.850-9C>T
NM_001303405.2:c.439-9C>T	NP_001290334.1:n.439-9C>T
NM_001303406.2:c.439-9C>T	NP_001290335.1:n.439-9C>T
NM_001303407.2:c.115-9C>T	NP_001290336.1:n.115-9C>T