Canonical Allele Identifier: CA410569727

Gene: PCNT

Linked Data

• MyVariant Identifiers: chr21:g.47786857C>G (hg19) ; chr21:g.46366942C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46366942C>G , CM000683.2:g.46366942C>G	GRCh38
NC_000021.8:g.47786857C>G , CM000683.1:g.47786857C>G	GRCh37
NC_000021.7:g.46611285C>G	NCBI36
NG_008961.1:g.47822C>G
NG_008961.2:g.47821C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1464C>G	ENSP00000511987.1:n.*1464C>G
ENST00000695525.1:n.3054C>G
ENST00000695558.1:c.2968C>G	ENSP00000512015.1:p.Leu990Val
ENST00000703224.1:c.*2211C>G	ENSP00000515242.1:n.*2211C>G
ENST00000359568.10:c.2968C>G MANE Select	ENSP00000352572.5:p.Leu990Val
ENST00000359568.9:c.2968C>G	ENSP00000352572.5:p.Leu990Val
ENST00000480896.5:n.3237C>G
NM_001315529.1:c.2614C>G	NP_001302458.1:p.Leu872Val
NM_006031.5:c.2968C>G	NP_006022.3:p.Leu990Val
XM_005261124.3:c.2968C>G	XP_005261181.1:p.Leu990Val
XM_011529593.1:c.3049C>G	XP_011527895.1:p.Leu1017Val
XM_011529594.1:c.3049C>G	XP_011527896.1:p.Leu1017Val
XM_005261124.5:c.2968C>G	XP_005261181.1:p.Leu990Val
XM_011529594.3:c.3049C>G	XP_011527896.1:p.Leu1017Val
XM_017028362.2:c.2968C>G	XP_016883851.1:p.Leu990Val
XM_017028363.1:c.2614C>G	XP_016883852.1:p.Leu872Val
XM_024452082.1:c.1852C>G	XP_024307850.1:p.Leu618Val
XM_024452083.1:c.748C>G	XP_024307851.1:p.Leu250Val
NM_006031.6:c.2968C>G MANE Select	NP_006022.3:p.Leu990Val
NM_001315529.2:c.2614C>G	NP_001302458.1:p.Leu872Val