Canonical Allele Identifier: CA974002907

Gene: ZNF500

Linked Data

• gnomAD v3: 16-4762412-C-CTTTTT
• gnomAD v4: 16-4762412-C-CTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762412_4762413insTTTTT , CM000678.2:g.4762412_4762413insTTTTT	GRCh38
NC_000016.9:g.4812413_4812414insTTTTT , CM000678.1:g.4812413_4812414insTTTTT	GRCh37
NC_000016.8:g.4752414_4752415insTTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.599-78_599-77insAAAAA MANE Select	ENSP00000219478.5:n.599-78_599-77insAAAAA
ENST00000219478.10:c.599-78_599-77insAAAAA	ENSP00000219478.5:n.599-78_599-77insAAAAA
ENST00000545009.1:c.599-78_599-77insAAAAA	ENSP00000445714.1:n.599-78_599-77insAAAAA
ENST00000589422.1:c.*127-78_*127-77insAAAAA	ENSP00000466375.1:n.*127-78_*127-77insAAAAA
NM_001303450.1:c.599-78_599-77insAAAAA	NP_001290379.1:n.599-78_599-77insAAAAA
NM_021646.2:c.599-78_599-77insAAAAA	NP_067678.1:n.599-78_599-77insAAAAA
XM_005255243.2:c.248-78_248-77insAAAAA	XP_005255300.1:n.248-78_248-77insAAAAA
XM_011522453.1:c.599-78_599-77insAAAAA	XP_011520755.1:n.599-78_599-77insAAAAA
XM_011522454.1:c.-26-78_-26-77insAAAAA	XP_011520756.1:n.-26-78_-26-77insAAAAA
NM_021646.3:c.599-78_599-77insAAAAA	NP_067678.1:n.599-78_599-77insAAAAA
XM_005255243.4:c.248-78_248-77insAAAAA	XP_005255300.1:n.248-78_248-77insAAAAA
XM_011522453.2:c.599-78_599-77insAAAAA	XP_011520755.1:n.599-78_599-77insAAAAA
XM_011522454.3:c.-26-78_-26-77insAAAAA	XP_011520756.1:n.-26-78_-26-77insAAAAA
XM_017023121.2:c.-26-78_-26-77insAAAAA	XP_016878610.1:n.-26-78_-26-77insAAAAA
NM_001303450.2:c.599-78_599-77insAAAAA	NP_001290379.1:n.599-78_599-77insAAAAA
NM_021646.4:c.599-78_599-77insAAAAA MANE Select	NP_067678.1:n.599-78_599-77insAAAAA