Canonical Allele Identifier: CA9884816

Gene: ZNF335

Linked Data

• ClinVar Variation Id: 437354
• ClinVar RCV Id: RCV000504231 ; RCV000903824 ; RCV002244977
• dbSNP Id: rs150750750
• ExAC: 20:44577895 AGG / A
• gnomAD v2: 20-44577895-AGG-A
• gnomAD v3: 20-45949256-AGG-A
• gnomAD v4: 20-45949256-AGG-A
• MyVariant Identifiers: chr20:g.44577896_44577897del (hg19) ; chr20:g.45949258_45949259del (hg38) ; chr20:g.45949257_45949258del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45949259_45949260del , CM000682.2:g.45949259_45949260del	GRCh38
NC_000020.10:g.44577898_44577899del , CM000682.1:g.44577898_44577899del	GRCh37
NC_000020.9:g.44011305_44011306del	NCBI36
NG_029772.1:g.27937_27938del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322927.3:c.3820-7_3820-6del MANE Select	ENSP00000325326.2:n.3820-7_3820-6del
ENST00000322927.2:c.3820-7_3820-6del	ENSP00000325326.2:n.3820-7_3820-6del
NM_022095.3:c.3820-7_3820-6del	NP_071378.1:n.3820-7_3820-6del
XM_005260504.3:c.3817-7_3817-6del	XP_005260561.1:n.3817-7_3817-6del
XM_005260506.2:c.3292-7_3292-6del	XP_005260563.1:n.3292-7_3292-6del
XM_005260504.4:c.3817-7_3817-6del	XP_005260561.1:n.3817-7_3817-6del
XM_017028012.1:c.3292-7_3292-6del	XP_016883501.1:n.3292-7_3292-6del
XR_002958500.1:n.5767-7_5767-6del
XR_002958501.1:n.4447-7_4447-6del
XR_936602.3:n.4331-7_4331-6del
NM_022095.4:c.3820-7_3820-6del MANE Select	NP_071378.1:n.3820-7_3820-6del