Canonical Allele Identifier: CA2344035330

Gene: ZNF71

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.56620870C= , CM000681.2:g.56620870C=	GRCh38
NC_000019.9:g.57132238C= , CM000681.1:g.57132238C=	GRCh37
NC_000019.8:g.61824050C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001370215.1:c.161-398C= MANE Select	NP_001357144.1:n.161-398C=
ENST00000599599.7:c.161-398C= MANE Select	ENSP00000471138.2:n.161-398C=
NM_001370214.1:c.-20-398C=	NP_001357143.1:n.-20-398C=
NM_021216.4:c.-20-398C=	NP_067039.1:n.-20-398C=
NM_021216.5:c.-20-398C=	NP_067039.1:n.-20-398C=
NR_163262.1:n.339+6932C=
NR_163263.1:n.212+19279C=
ENST00000328070.10:c.-20-398C=	ENSP00000328245.5:n.-20-398C=
ENST00000599599.5:c.-20-398C=	ENSP00000471138.1:n.-20-398C=
XM_011527193.1:c.161-398C=	XP_011525495.1:n.161-398C=
XM_011527193.2:c.161-398C=	XP_011525495.1:n.161-398C=
XM_017027078.1:c.161-398C=	XP_016882567.1:n.161-398C=
XM_017027079.1:c.161-398C=	XP_016882568.1:n.161-398C=
XM_017027080.1:c.-20-398C=	XP_016882569.1:n.-20-398C=