Canonical Allele Identifier: CA410570209

Gene: PCNT

Linked Data

• dbSNP Id: rs1320302184
• gnomAD v2: 21-47786940-G-C
• gnomAD v4: 21-46367025-G-C
• MyVariant Identifiers: chr21:g.47786940G>C (hg19) ; chr21:g.46367025G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367025G>C , CM000683.2:g.46367025G>C	GRCh38
NC_000021.8:g.47786940G>C , CM000683.1:g.47786940G>C	GRCh37
NC_000021.7:g.46611368G>C	NCBI36
NG_008961.1:g.47905G>C
NG_008961.2:g.47904G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1547G>C	ENSP00000511987.1:n.*1547G>C
ENST00000695525.1:n.3137G>C
ENST00000695558.1:c.3051G>C	ENSP00000512015.1:p.Glu1017Asp
ENST00000703224.1:c.*2294G>C	ENSP00000515242.1:n.*2294G>C
ENST00000359568.10:c.3051G>C MANE Select	ENSP00000352572.5:p.Glu1017Asp
ENST00000359568.9:c.3051G>C	ENSP00000352572.5:p.Glu1017Asp
ENST00000480896.5:n.3320G>C
NM_001315529.1:c.2697G>C	NP_001302458.1:p.Glu899Asp
NM_006031.5:c.3051G>C	NP_006022.3:p.Glu1017Asp
XM_005261124.3:c.3051G>C	XP_005261181.1:p.Glu1017Asp
XM_011529593.1:c.3132G>C	XP_011527895.1:p.Glu1044Asp
XM_011529594.1:c.3132G>C	XP_011527896.1:p.Glu1044Asp
XM_005261124.5:c.3051G>C	XP_005261181.1:p.Glu1017Asp
XM_011529594.3:c.3132G>C	XP_011527896.1:p.Glu1044Asp
XM_017028362.2:c.3051G>C	XP_016883851.1:p.Glu1017Asp
XM_017028363.1:c.2697G>C	XP_016883852.1:p.Glu899Asp
XM_024452082.1:c.1935G>C	XP_024307850.1:p.Glu645Asp
XM_024452083.1:c.831G>C	XP_024307851.1:p.Glu277Asp
NM_006031.6:c.3051G>C MANE Select	NP_006022.3:p.Glu1017Asp
NM_001315529.2:c.2697G>C	NP_001302458.1:p.Glu899Asp