Canonical Allele Identifier: CA410569970

Gene: PCNT

Linked Data

• gnomAD v4: 21-46366986-G-C
• MyVariant Identifiers: chr21:g.47786901G>C (hg19) ; chr21:g.46366986G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46366986G>C , CM000683.2:g.46366986G>C	GRCh38
NC_000021.8:g.47786901G>C , CM000683.1:g.47786901G>C	GRCh37
NC_000021.7:g.46611329G>C	NCBI36
NG_008961.1:g.47866G>C
NG_008961.2:g.47865G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1508G>C	ENSP00000511987.1:n.*1508G>C
ENST00000695525.1:n.3098G>C
ENST00000695558.1:c.3012G>C	ENSP00000512015.1:p.Lys1004Asn
ENST00000703224.1:c.*2255G>C	ENSP00000515242.1:n.*2255G>C
ENST00000359568.10:c.3012G>C MANE Select	ENSP00000352572.5:p.Lys1004Asn
ENST00000359568.9:c.3012G>C	ENSP00000352572.5:p.Lys1004Asn
ENST00000480896.5:n.3281G>C
NM_001315529.1:c.2658G>C	NP_001302458.1:p.Lys886Asn
NM_006031.5:c.3012G>C	NP_006022.3:p.Lys1004Asn
XM_005261124.3:c.3012G>C	XP_005261181.1:p.Lys1004Asn
XM_011529593.1:c.3093G>C	XP_011527895.1:p.Lys1031Asn
XM_011529594.1:c.3093G>C	XP_011527896.1:p.Lys1031Asn
XM_005261124.5:c.3012G>C	XP_005261181.1:p.Lys1004Asn
XM_011529594.3:c.3093G>C	XP_011527896.1:p.Lys1031Asn
XM_017028362.2:c.3012G>C	XP_016883851.1:p.Lys1004Asn
XM_017028363.1:c.2658G>C	XP_016883852.1:p.Lys886Asn
XM_024452082.1:c.1896G>C	XP_024307850.1:p.Lys632Asn
XM_024452083.1:c.792G>C	XP_024307851.1:p.Lys264Asn
NM_006031.6:c.3012G>C MANE Select	NP_006022.3:p.Lys1004Asn
NM_001315529.2:c.2658G>C	NP_001302458.1:p.Lys886Asn