Canonical Allele Identifier: CA394621353

Gene: ZNF500

Linked Data

• MyVariant Identifiers: chr16:g.4812747A>G (hg19) ; chr16:g.4762746A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762746A>G , CM000678.2:g.4762746A>G	GRCh38
NC_000016.9:g.4812747A>G , CM000678.1:g.4812747A>G	GRCh37
NC_000016.8:g.4752748A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.425T>C MANE Select	ENSP00000219478.5:p.Leu142Pro
ENST00000219478.10:c.425T>C	ENSP00000219478.5:p.Leu142Pro
ENST00000545009.1:c.425T>C	ENSP00000445714.1:p.Leu142Pro
ENST00000589422.1:c.415-33T>C	ENSP00000466375.1:n.415-33T>C
NM_001303450.1:c.425T>C	NP_001290379.1:p.Leu142Pro
NM_021646.2:c.425T>C	NP_067678.1:p.Leu142Pro
XM_005255243.2:c.74T>C	XP_005255300.1:p.Leu25Pro
XM_011522453.1:c.425T>C	XP_011520755.1:p.Leu142Pro
XM_011522454.1:c.-167-33T>C	XP_011520756.1:n.-167-33T>C
NM_021646.3:c.425T>C	NP_067678.1:p.Leu142Pro
XM_005255243.4:c.74T>C	XP_005255300.1:p.Leu25Pro
XM_011522453.2:c.425T>C	XP_011520755.1:p.Leu142Pro
XM_011522454.3:c.-167-33T>C	XP_011520756.1:n.-167-33T>C
XM_017023121.2:c.-200T>C	XP_016878610.1:n.-200T>C
NM_001303450.2:c.425T>C	NP_001290379.1:p.Leu142Pro
NM_021646.4:c.425T>C MANE Select	NP_067678.1:p.Leu142Pro