Canonical Allele Identifier: CA2631540200

Gene: ZNF500

Linked Data

• gnomAD v4: 16-4762422-G-GATAAAAGAAAAAGAAACTTGGCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762422_4762423insATAAAAGAAAAAGAAACTTGGCCA , CM000678.2:g.4762422_4762423insATAAAAGAAAAAGAAACTTGGCCA	GRCh38
NC_000016.9:g.4812423_4812424insATAAAAGAAAAAGAAACTTGGCCA , CM000678.1:g.4812423_4812424insATAAAAGAAAAAGAAACTTGGCCA	GRCh37
NC_000016.8:g.4752424_4752425insATAAAAGAAAAAGAAACTTGGCCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT MANE Select	ENSP00000219478.5:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT
ENST00000219478.10:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT	ENSP00000219478.5:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT
ENST00000545009.1:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT	ENSP00000445714.1:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT
ENST00000589422.1:c.*127-88_*127-87insTGGCCAAGTTTCTTTTTCTTTTAT	ENSP00000466375.1:n.*127-88_*127-87insTGGCCAAGTTTCTTTTTCTTTTA...
NM_001303450.1:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT	NP_001290379.1:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT
NM_021646.2:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT	NP_067678.1:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT
XM_005255243.2:c.248-88_248-87insTGGCCAAGTTTCTTTTTCTTTTAT	XP_005255300.1:n.248-88_248-87insTGGCCAAGTTTCTTTTTCTTTTAT
XM_011522453.1:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT	XP_011520755.1:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT
XM_011522454.1:c.-26-88_-26-87insTGGCCAAGTTTCTTTTTCTTTTAT	XP_011520756.1:n.-26-88_-26-87insTGGCCAAGTTTCTTTTTCTTTTAT
NM_021646.3:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT	NP_067678.1:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT
XM_005255243.4:c.248-88_248-87insTGGCCAAGTTTCTTTTTCTTTTAT	XP_005255300.1:n.248-88_248-87insTGGCCAAGTTTCTTTTTCTTTTAT
XM_011522453.2:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT	XP_011520755.1:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT
XM_011522454.3:c.-26-88_-26-87insTGGCCAAGTTTCTTTTTCTTTTAT	XP_011520756.1:n.-26-88_-26-87insTGGCCAAGTTTCTTTTTCTTTTAT
XM_017023121.2:c.-26-88_-26-87insTGGCCAAGTTTCTTTTTCTTTTAT	XP_016878610.1:n.-26-88_-26-87insTGGCCAAGTTTCTTTTTCTTTTAT
NM_001303450.2:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT	NP_001290379.1:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT
NM_021646.4:c.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT MANE Select	NP_067678.1:n.599-88_599-87insTGGCCAAGTTTCTTTTTCTTTTAT