Canonical Allele Identifier: CA883364782

Gene: ZNF610

Linked Data

• dbSNP Id: rs1249368490
• MyVariant Identifiers: chr19:g.52863795del (hg19) ; chr19:g.52360542del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52360543del , CM000681.2:g.52360543del	GRCh38
NC_000019.9:g.52863796del , CM000681.1:g.52863796del	GRCh37
NC_000019.8:g.57555608del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000403906.8:c.320-5155del MANE Select	ENSP00000383922.2:n.320-5155del
ENST00000321287.12:c.320-5155del	ENSP00000324441.8:n.320-5155del
ENST00000327920.12:c.320-5155del	ENSP00000327597.7:n.320-5155del
ENST00000403906.7:c.320-5155del	ENSP00000383922.2:n.320-5155del
ENST00000601151.5:c.191-5155del	ENSP00000471021.1:n.191-5155del
ENST00000613461.3:c.191-5155del	ENSP00000477617.1:n.191-5155del
ENST00000616431.2:c.320-5155del	ENSP00000485001.1:n.320-5155del
NM_001161425.1:c.320-5155del	NP_001154897.1:n.320-5155del
NM_001161426.1:c.320-5155del	NP_001154898.1:n.320-5155del
NM_001161427.1:c.191-5155del	NP_001154899.1:n.191-5155del
NM_173530.2:c.320-5155del	NP_775801.2:n.320-5155del
XM_011526560.1:c.320-5155del	XP_011524862.1:n.320-5155del
XM_011526561.1:c.320-5155del	XP_011524863.1:n.320-5155del
XM_011526562.1:c.320-5155del	XP_011524864.1:n.320-5155del
NM_001161425.2:c.320-5155del MANE Select	NP_001154897.1:n.320-5155del
NM_001161426.2:c.320-5155del	NP_001154898.1:n.320-5155del
NM_001161427.2:c.191-5155del	NP_001154899.1:n.191-5155del
NM_173530.3:c.320-5155del	NP_775801.2:n.320-5155del