Canonical Allele Identifier: CA2631540574

Gene: ZNF500

Linked Data

• gnomAD v4: 16-4762774-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762774T>G , CM000678.2:g.4762774T>G	GRCh38
NC_000016.9:g.4812775T>G , CM000678.1:g.4812775T>G	GRCh37
NC_000016.8:g.4752776T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.415-18A>C MANE Select	ENSP00000219478.5:n.415-18A>C
ENST00000219478.10:c.415-18A>C	ENSP00000219478.5:n.415-18A>C
ENST00000545009.1:c.415-18A>C	ENSP00000445714.1:n.415-18A>C
ENST00000589422.1:c.415-61A>C	ENSP00000466375.1:n.415-61A>C
NM_001303450.1:c.415-18A>C	NP_001290379.1:n.415-18A>C
NM_021646.2:c.415-18A>C	NP_067678.1:n.415-18A>C
XM_005255243.2:c.64-18A>C	XP_005255300.1:n.64-18A>C
XM_011522453.1:c.415-18A>C	XP_011520755.1:n.415-18A>C
XM_011522454.1:c.-167-61A>C	XP_011520756.1:n.-167-61A>C
NM_021646.3:c.415-18A>C	NP_067678.1:n.415-18A>C
XM_005255243.4:c.64-18A>C	XP_005255300.1:n.64-18A>C
XM_011522453.2:c.415-18A>C	XP_011520755.1:n.415-18A>C
XM_011522454.3:c.-167-61A>C	XP_011520756.1:n.-167-61A>C
XM_017023121.2:c.-210-18A>C	XP_016878610.1:n.-210-18A>C
NM_001303450.2:c.415-18A>C	NP_001290379.1:n.415-18A>C
NM_021646.4:c.415-18A>C MANE Select	NP_067678.1:n.415-18A>C