Canonical Allele Identifier: CA1622076894

Gene: ZFAND3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38068644A= , CM000668.2:g.38068644A=	GRCh38
NC_000006.11:g.38036420A= , CM000668.1:g.38036420A=	GRCh37
NC_000006.10:g.38144398A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287218.9:c.295+6869A= MANE Select	ENSP00000287218.4:n.295+6869A=
ENST00000287218.8:c.295+6869A=	ENSP00000287218.4:n.295+6869A=
ENST00000373389.5:c.224+6869A=
ENST00000373391.6:c.295+6869A=	ENSP00000362489.2:n.295+6869A=
ENST00000474522.5:c.388+6869A=	ENSP00000420240.1:n.388+6869A=
NM_021943.2:c.295+6869A=	NP_068762.1:n.295+6869A=
XM_005249269.1:c.295+6869A=	XP_005249326.1:n.295+6869A=
XM_006715155.2:c.295+6869A=	XP_006715218.1:n.295+6869A=
XM_011514790.1:c.295+6869A=	XP_011513092.1:n.295+6869A=
XM_005249269.2:c.295+6869A=	XP_005249326.1:n.295+6869A=
XM_011514790.2:c.295+6869A=	XP_011513092.1:n.295+6869A=
XM_017011171.2:c.247+6869A=	XP_016866660.1:n.247+6869A=
NM_021943.3:c.295+6869A= MANE Select	NP_068762.1:n.295+6869A=