Canonical Allele Identifier: CA394770963

Gene: ZC3H7A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11756290T>C , CM000678.2:g.11756290T>C	GRCh38
NC_000016.9:g.11850146T>C , CM000678.1:g.11850146T>C	GRCh37
NC_000016.8:g.11757647T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014153.4:c.2509A>G MANE Select	NP_054872.2:p.Asn837Asp
ENST00000355758.9:c.2509A>G MANE Select	ENSP00000347999.4:p.Asn837Asp
NM_014153.3:c.2509A>G	NP_054872.2:p.Asn837Asp
ENST00000355758.8:c.2509A>G	ENSP00000347999.4:p.Asn837Asp
ENST00000396516.6:c.2509A>G	ENSP00000379773.2:p.Asn837Asp
ENST00000571405.5:c.801A>G
ENST00000575984.1:c.97A>G	ENSP00000459477.1:p.Asn33Asp
XM_005255273.2:c.1336A>G	XP_005255330.1:p.Asn446Asp
XM_006720877.2:c.2509A>G	XP_006720940.1:p.Asn837Asp
XM_011522463.1:c.2509A>G	XP_011520765.1:p.Asn837Asp
XM_011522463.2:c.2509A>G	XP_011520765.1:p.Asn837Asp
XM_011522464.1:c.1792A>G	XP_011520766.1:p.Asn598Asp
XM_011522464.2:c.1792A>G	XP_011520766.1:p.Asn598Asp
XM_017023174.1:c.2206A>G	XP_016878663.1:p.Asn736Asp
XM_024450243.1:c.1336A>G	XP_024306011.1:p.Asn446Asp
XR_932825.1:n.2572A>G