Canonical Allele Identifier: CA2580099007

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46398015_46399797del , CM000683.2:g.46398015_46399797del	GRCh38
NC_000021.8:g.47817929_47819711del , CM000683.1:g.47817929_47819711del	GRCh37
NC_000021.7:g.46642357_46644139del	NCBI36
NG_008961.1:g.78894_80676del
NG_008961.2:g.78894_80676del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695558.1:c.4481_4824+1del
ENST00000703224.1:c.*3691_*4034+1del
ENST00000359568.10:c.4448_4791+1del
ENST00000359568.9:c.4448_4791+1del
ENST00000480896.5:n.4717_5060+1del
NM_001315529.1:c.4094_4437+1del
NM_006031.5:c.4448_4791+1del
XM_005261124.3:c.4481_4824+1del
XM_011529593.1:c.4562_4902+1del
XM_011529594.1:c.4529_4872+1del
XM_005261124.5:c.4481_4824+1del
XM_011529594.3:c.4529_4872+1del
XM_017028362.2:c.4448_4791+1del
XM_017028363.1:c.4127_4470+1del
XM_024452082.1:c.3365_3708+1del
XM_024452083.1:c.2261_2604+1del
NM_006031.6:c.4448_4791+1del
NM_001315529.2:c.4094_4437+1del