Canonical Allele Identifier: CA410555854

Gene: PCNT

Linked Data

• MyVariant Identifiers: chr21:g.47831658C>G (hg19) ; chr21:g.46411744C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46411744C>G , CM000683.2:g.46411744C>G	GRCh38
NC_000021.8:g.47831658C>G , CM000683.1:g.47831658C>G	GRCh37
NC_000021.7:g.46656086C>G	NCBI36
NG_008961.1:g.92623C>G
NG_008961.2:g.92623C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695527.1:n.16C>G
ENST00000695558.1:c.5704C>G	ENSP00000512015.1:p.Leu1902Val
ENST00000703224.1:c.*4914C>G	ENSP00000515242.1:n.*4914C>G
ENST00000359568.10:c.5671C>G MANE Select	ENSP00000352572.5:p.Leu1891Val
ENST00000359568.9:c.5671C>G	ENSP00000352572.5:p.Leu1891Val
ENST00000480896.5:n.5940C>G
NM_001315529.1:c.5317C>G	NP_001302458.1:p.Leu1773Val
NM_006031.5:c.5671C>G	NP_006022.3:p.Leu1891Val
XM_005261124.3:c.5704C>G	XP_005261181.1:p.Leu1902Val
XM_011529593.1:c.5782C>G	XP_011527895.1:p.Leu1928Val
XM_011529594.1:c.5752C>G	XP_011527896.1:p.Leu1918Val
XM_005261124.5:c.5704C>G	XP_005261181.1:p.Leu1902Val
XM_011529594.3:c.5752C>G	XP_011527896.1:p.Leu1918Val
XM_017028362.2:c.5671C>G	XP_016883851.1:p.Leu1891Val
XM_017028363.1:c.5350C>G	XP_016883852.1:p.Leu1784Val
XM_024452082.1:c.4588C>G	XP_024307850.1:p.Leu1530Val
XM_024452083.1:c.3484C>G	XP_024307851.1:p.Leu1162Val
NM_006031.6:c.5671C>G MANE Select	NP_006022.3:p.Leu1891Val
NM_001315529.2:c.5317C>G	NP_001302458.1:p.Leu1773Val