Canonical Allele Identifier: CA410570307

Gene: PCNT

Linked Data

• MyVariant Identifiers: chr21:g.47786958C>A (hg19) ; chr21:g.46367043C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367043C>A , CM000683.2:g.46367043C>A	GRCh38
NC_000021.8:g.47786958C>A , CM000683.1:g.47786958C>A	GRCh37
NC_000021.7:g.46611386C>A	NCBI36
NG_008961.1:g.47923C>A
NG_008961.2:g.47922C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1565C>A	ENSP00000511987.1:n.*1565C>A
ENST00000695525.1:n.3155C>A
ENST00000695558.1:c.3069C>A	ENSP00000512015.1:p.His1023Gln
ENST00000703224.1:c.*2312C>A	ENSP00000515242.1:n.*2312C>A
ENST00000359568.10:c.3069C>A MANE Select	ENSP00000352572.5:p.His1023Gln
ENST00000359568.9:c.3069C>A	ENSP00000352572.5:p.His1023Gln
ENST00000480896.5:n.3338C>A
NM_001315529.1:c.2715C>A	NP_001302458.1:p.His905Gln
NM_006031.5:c.3069C>A	NP_006022.3:p.His1023Gln
XM_005261124.3:c.3069C>A	XP_005261181.1:p.His1023Gln
XM_011529593.1:c.3150C>A	XP_011527895.1:p.His1050Gln
XM_011529594.1:c.3150C>A	XP_011527896.1:p.His1050Gln
XM_005261124.5:c.3069C>A	XP_005261181.1:p.His1023Gln
XM_011529594.3:c.3150C>A	XP_011527896.1:p.His1050Gln
XM_017028362.2:c.3069C>A	XP_016883851.1:p.His1023Gln
XM_017028363.1:c.2715C>A	XP_016883852.1:p.His905Gln
XM_024452082.1:c.1953C>A	XP_024307850.1:p.His651Gln
XM_024452083.1:c.849C>A	XP_024307851.1:p.His283Gln
NM_006031.6:c.3069C>A MANE Select	NP_006022.3:p.His1023Gln
NM_001315529.2:c.2715C>A	NP_001302458.1:p.His905Gln