Canonical Allele Identifier: CA512734435

Gene: PCNT

Linked Data

• gnomAD v4: 21-46367034-G-A
• MyVariant Identifiers: chr21:g.47786949G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367034G>A , CM000683.2:g.46367034G>A	GRCh38
NC_000021.8:g.47786949G>A , CM000683.1:g.47786949G>A	GRCh37
NC_000021.7:g.46611377G>A	NCBI36
NG_008961.1:g.47914G>A
NG_008961.2:g.47913G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1556G>A	ENSP00000511987.1:n.*1556G>A
ENST00000695525.1:n.3146G>A
ENST00000695558.1:c.3060G>A	ENSP00000512015.1:p.Lys1020=
ENST00000703224.1:c.*2303G>A	ENSP00000515242.1:n.*2303G>A
ENST00000359568.10:c.3060G>A MANE Select	ENSP00000352572.5:p.Lys1020=
ENST00000359568.9:c.3060G>A	ENSP00000352572.5:p.Lys1020=
ENST00000480896.5:n.3329G>A
NM_001315529.1:c.2706G>A	NP_001302458.1:p.Lys902=
NM_006031.5:c.3060G>A	NP_006022.3:p.Lys1020=
XM_005261124.3:c.3060G>A	XP_005261181.1:p.Lys1020=
XM_011529593.1:c.3141G>A	XP_011527895.1:p.Lys1047=
XM_011529594.1:c.3141G>A	XP_011527896.1:p.Lys1047=
XM_005261124.5:c.3060G>A	XP_005261181.1:p.Lys1020=
XM_011529594.3:c.3141G>A	XP_011527896.1:p.Lys1047=
XM_017028362.2:c.3060G>A	XP_016883851.1:p.Lys1020=
XM_017028363.1:c.2706G>A	XP_016883852.1:p.Lys902=
XM_024452082.1:c.1944G>A	XP_024307850.1:p.Lys648=
XM_024452083.1:c.840G>A	XP_024307851.1:p.Lys280=
NM_006031.6:c.3060G>A MANE Select	NP_006022.3:p.Lys1020=
NM_001315529.2:c.2706G>A	NP_001302458.1:p.Lys902=