Canonical Allele Identifier: CA2339233387

Gene: ZC3H4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47097184G= , CM000681.2:g.47097184G=	GRCh38
NC_000019.9:g.47600441G= , CM000681.1:g.47600441G=	GRCh37
NC_000019.8:g.52292281G=	NCBI36
NG_027798.1:g.21569C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015168.2:c.162-2576C= MANE Select	NP_055983.1:n.162-2576C=
ENST00000253048.10:c.162-2576C= MANE Select	ENSP00000253048.4:n.162-2576C=
NM_015168.1:c.162-2576C=	NP_055983.1:n.162-2576C=
ENST00000253048.9:c.162-2576C=	ENSP00000253048.4:n.162-2576C=
ENST00000594019.5:n.83-2576C=
ENST00000597069.1:n.163-2576C=
XM_005258676.3:c.-328C=	XP_005258733.1:n.-328C=
XM_005258677.3:c.39-2576C=	XP_005258734.1:n.39-2576C=
XM_005258677.4:c.39-2576C=	XP_005258734.1:n.39-2576C=
XM_005258678.1:c.15-2576C=	XP_005258735.1:n.15-2576C=
XM_005258678.2:c.15-2576C=	XP_005258735.1:n.15-2576C=
XM_006723113.2:c.162-2576C=	XP_006723176.1:n.162-2576C=
XM_006723113.3:c.162-2576C=	XP_006723176.1:n.162-2576C=
XM_011526668.1:c.39-2576C=	XP_011524970.1:n.39-2576C=
XM_011526668.3:c.39-2576C=	XP_011524970.1:n.39-2576C=
XM_011526669.1:c.24-2576C=	XP_011524971.1:n.24-2576C=
XM_011526669.3:c.24-2576C=	XP_011524971.1:n.24-2576C=
XM_011526670.1:c.12-2576C=	XP_011524972.1:n.12-2576C=
XM_011526670.3:c.12-2576C=	XP_011524972.1:n.12-2576C=
XM_017026530.2:c.162-2576C=	XP_016882019.1:n.162-2576C=
XM_017026531.1:c.-575-2576C=	XP_016882020.1:n.-575-2576C=