Canonical Allele Identifier: CA1743051465

Gene: ZC3HC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.130023656C= , CM000669.2:g.130023656C=	GRCh38
NC_000007.13:g.129663496C= , CM000669.1:g.129663496C=	GRCh37
NC_000007.12:g.129450732C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358303.9:c.1088G= MANE Select	ENSP00000351052.4:p.Arg363=
ENST00000648450.1:c.*1098G=	ENSP00000498166.1:n.*1098G=
ENST00000311873.9:c.1025G=	ENSP00000309301.5:p.Arg342=
ENST00000358303.8:c.1088G=	ENSP00000351052.4:p.Arg363=
ENST00000360708.9:c.1020+607G=	ENSP00000353933.5:n.1020+607G=
ENST00000467642.5:c.*972G=	ENSP00000419509.1:n.*972G=
ENST00000477578.5:n.758G=
ENST00000481503.5:c.959G=	ENSP00000418533.1:p.Arg320=
NM_001282190.1:c.1025G=	NP_001269119.1:p.Arg342=
NM_001282191.1:c.1020+607G=	NP_001269120.1:n.1020+607G=
NM_016478.4:c.1088G=	NP_057562.3:p.Arg363=
XM_005250403.1:c.716G=	XP_005250460.1:p.Arg239=
XM_011516288.1:c.887G=	XP_011514590.1:p.Arg296=
XM_011516289.1:c.818G=	XP_011514591.1:p.Arg273=
XM_011516290.1:c.584G=	XP_011514592.1:p.Arg195=
NM_001363701.1:c.959G=	NP_001350630.1:p.Arg320=
XM_005250403.3:c.716G=	XP_005250460.1:p.Arg239=
XM_011516288.3:c.887G=	XP_011514590.1:p.Arg296=
XM_011516289.2:c.818G=	XP_011514591.1:p.Arg273=
XM_011516290.2:c.584G=	XP_011514592.1:p.Arg195=
XM_017012288.1:c.584G=	XP_016867777.1:p.Arg195=
XM_024446792.1:c.749G=	XP_024302560.1:p.Arg250=
NM_016478.5:c.1088G= MANE Select	NP_057562.3:p.Arg363=
NM_001282190.2:c.1025G=	NP_001269119.1:p.Arg342=