Canonical Allele Identifier: CA2581370338

Gene: ZNF627

Genomic Alleles

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

Transcript Alleles

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