Canonical Allele Identifier: CA410570394

Gene: PCNT

Linked Data

• MyVariant Identifiers: chr21:g.47786972A>C (hg19) ; chr21:g.46367057A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367057A>C , CM000683.2:g.46367057A>C	GRCh38
NC_000021.8:g.47786972A>C , CM000683.1:g.47786972A>C	GRCh37
NC_000021.7:g.46611400A>C	NCBI36
NG_008961.1:g.47937A>C
NG_008961.2:g.47936A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1579A>C	ENSP00000511987.1:n.*1579A>C
ENST00000695525.1:n.3169A>C
ENST00000695558.1:c.3083A>C	ENSP00000512015.1:p.Gln1028Pro
ENST00000703224.1:c.*2326A>C	ENSP00000515242.1:n.*2326A>C
ENST00000359568.10:c.3083A>C MANE Select	ENSP00000352572.5:p.Gln1028Pro
ENST00000359568.9:c.3083A>C	ENSP00000352572.5:p.Gln1028Pro
ENST00000480896.5:n.3352A>C
NM_001315529.1:c.2729A>C	NP_001302458.1:p.Gln910Pro
NM_006031.5:c.3083A>C	NP_006022.3:p.Gln1028Pro
XM_005261124.3:c.3083A>C	XP_005261181.1:p.Gln1028Pro
XM_011529593.1:c.3164A>C	XP_011527895.1:p.Gln1055Pro
XM_011529594.1:c.3164A>C	XP_011527896.1:p.Gln1055Pro
XM_005261124.5:c.3083A>C	XP_005261181.1:p.Gln1028Pro
XM_011529594.3:c.3164A>C	XP_011527896.1:p.Gln1055Pro
XM_017028362.2:c.3083A>C	XP_016883851.1:p.Gln1028Pro
XM_017028363.1:c.2729A>C	XP_016883852.1:p.Gln910Pro
XM_024452082.1:c.1967A>C	XP_024307850.1:p.Gln656Pro
XM_024452083.1:c.863A>C	XP_024307851.1:p.Gln288Pro
NM_006031.6:c.3083A>C MANE Select	NP_006022.3:p.Gln1028Pro
NM_001315529.2:c.2729A>C	NP_001302458.1:p.Gln910Pro