Canonical Allele Identifier: CA9622762

Gene: ZNF610

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52366481C>T , CM000681.2:g.52366481C>T	GRCh38
NC_000019.9:g.52869734C>T , CM000681.1:g.52869734C>T	GRCh37
NC_000019.8:g.57561546C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001161425.2:c.1103C>T MANE Select	NP_001154897.1:p.Thr368Ile
ENST00000403906.8:c.1103C>T MANE Select	ENSP00000383922.2:p.Thr368Ile
NM_001161425.1:c.1103C>T	NP_001154897.1:p.Thr368Ile
NM_001161426.1:c.1103C>T	NP_001154898.1:p.Thr368Ile
NM_001161426.2:c.1103C>T	NP_001154898.1:p.Thr368Ile
NM_001161427.1:c.974C>T	NP_001154899.1:p.Thr325Ile
NM_001161427.2:c.974C>T	NP_001154899.1:p.Thr325Ile
NM_173530.2:c.1103C>T	NP_775801.2:p.Thr368Ile
NM_173530.3:c.1103C>T	NP_775801.2:p.Thr368Ile
ENST00000321287.12:c.1103C>T	ENSP00000324441.8:p.Thr368Ile
ENST00000327920.12:c.1103C>T	ENSP00000327597.7:p.Thr368Ile
ENST00000403906.7:c.1103C>T	ENSP00000383922.2:p.Thr368Ile
ENST00000601151.5:c.974C>T	ENSP00000471021.1:p.Thr325Ile
ENST00000613461.3:c.974C>T	ENSP00000477617.1:p.Thr325Ile
ENST00000616431.2:c.1103C>T	ENSP00000485001.1:p.Thr368Ile
XM_011526560.1:c.1103C>T	XP_011524862.1:p.Thr368Ile
XM_011526561.1:c.1103C>T	XP_011524863.1:p.Thr368Ile
XM_011526562.1:c.1103C>T	XP_011524864.1:p.Thr368Ile