Canonical Allele Identifier: CA2323025388

Gene: ZNF627

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11617987A= , CM000681.2:g.11617987A=	GRCh38
NC_000019.9:g.11728802A= , CM000681.1:g.11728802A=	GRCh37
NC_000019.8:g.11589802A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_145295.4:c.*98A= MANE Select	NP_660338.1:n.*98A=
ENST00000361113.10:c.*98A= MANE Select	ENSP00000354414.4:n.*98A=
NM_001290083.1:c.*98A=	NP_001277012.1:n.*98A=
NM_001290083.2:c.*98A=	NP_001277012.1:n.*98A=
NM_001290084.1:c.*98A=	NP_001277013.1:n.*98A=
NM_001290084.2:c.*98A=	NP_001277013.1:n.*98A=
NM_001290084.3:c.*98A=	NP_001277013.1:n.*98A=
NM_001290085.1:c.*98A=	NP_001277014.1:n.*98A=
NM_001290085.2:c.*98A=	NP_001277014.1:n.*98A=
NM_145295.3:c.*98A=	NP_660338.1:n.*98A=
ENST00000361113.9:c.*98A=	ENSP00000354414.4:n.*98A=
ENST00000588174.1:c.*1269A=	ENSP00000465841.1:n.*1269A=
XM_011527780.1:c.*98A=	XP_011526082.1:n.*98A=
XM_011527780.2:c.*98A=	XP_011526082.1:n.*98A=