Canonical Allele Identifier: CA2203508317

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762285_4762289delinsAAAGG , CM000678.2:g.4762285_4762289delinsAAAGG	GRCh38
NC_000016.9:g.4812286_4812290delinsAAAGG , CM000678.1:g.4812286_4812290delinsAAAGG	GRCh37
NC_000016.8:g.4752287_4752291delinsAAAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.645_649delinsCCTTT MANE Select	ENSP00000219478.5:p.Phe215=
ENST00000219478.10:c.645_649delinsCCTTT	ENSP00000219478.5:p.Phe215=
ENST00000545009.1:c.645_649delinsCCTTT	ENSP00000445714.1:p.Phe215=
ENST00000589422.1:c.*173_*177delinsCCTTT	ENSP00000466375.1:n.*173_*177delinsCCTTT
NM_001303450.1:c.645_649delinsCCTTT	NP_001290379.1:p.Phe215=
NM_021646.2:c.645_649delinsCCTTT	NP_067678.1:p.Phe215=
XM_005255243.2:c.294_298delinsCCTTT	XP_005255300.1:p.Phe98=
XM_011522453.1:c.645_649delinsCCTTT	XP_011520755.1:p.Phe215=
XM_011522454.1:c.21_25delinsCCTTT	XP_011520756.1:p.Phe7=
NM_021646.3:c.645_649delinsCCTTT	NP_067678.1:p.Phe215=
XM_005255243.4:c.294_298delinsCCTTT	XP_005255300.1:p.Phe98=
XM_011522453.2:c.645_649delinsCCTTT	XP_011520755.1:p.Phe215=
XM_011522454.3:c.21_25delinsCCTTT	XP_011520756.1:p.Phe7=
XM_017023121.2:c.21_25delinsCCTTT	XP_016878610.1:p.Phe7=
NM_001303450.2:c.645_649delinsCCTTT	NP_001290379.1:p.Phe215=
NM_021646.4:c.645_649delinsCCTTT MANE Select	NP_067678.1:p.Phe215=