Canonical Allele Identifier: CA2821519674

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921756T>C , CM000685.2:g.64921756T>C	GRCh38
NC_000023.10:g.64141636T>C , CM000685.1:g.64141636T>C	GRCh37
NC_000023.9:g.64058361T>C	NCBI36
NG_021200.1:g.59778A>G
NG_021200.2:g.117989A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.156+61A>G	ENSP00000515193.1:n.156+61A>G
ENST00000492653.6:c.225+61A>G	ENSP00000515192.1:n.225+61A>G
ENST00000703133.1:c.*799+61A>G	ENSP00000515188.1:n.*799+61A>G
ENST00000703136.1:c.*183+61A>G	ENSP00000515190.1:n.*183+61A>G
ENST00000374839.8:c.225+61A>G MANE Select	ENSP00000363972.3:n.225+61A>G
ENST00000337990.2:c.156+61A>G	ENSP00000338650.2:n.156+61A>G
ENST00000374839.7:c.225+61A>G	ENSP00000363972.3:n.225+61A>G
ENST00000447788.6:c.225+61A>G	ENSP00000399126.2:n.225+61A>G
ENST00000476032.1:n.466+61A>G
ENST00000488608.5:n.381+61A>G
ENST00000488831.5:n.213+61A>G
ENST00000492653.5:n.321+61A>G
NM_001178032.2:c.156+61A>G	NP_001171503.1:n.156+61A>G
NM_001178033.2:c.225+61A>G	NP_001171504.1:n.225+61A>G
NM_001243804.1:c.156+61A>G	NP_001230733.1:n.156+61A>G
NM_018684.3:c.225+61A>G	NP_061154.1:n.225+61A>G
NR_045044.1:n.636+61A>G
NM_018684.4:c.225+61A>G MANE Select	NP_061154.1:n.225+61A>G
NM_001178032.3:c.156+61A>G	NP_001171503.1:n.156+61A>G
NM_001243804.2:c.156+61A>G	NP_001230733.1:n.156+61A>G
NR_045044.2:n.553+61A>G
NM_001178033.3:c.225+61A>G	NP_001171504.1:n.225+61A>G