Canonical Allele Identifier: CA410570242

Gene: PCNT

Linked Data

• MyVariant Identifiers: chr21:g.47786945T>G (hg19) ; chr21:g.46367030T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367030T>G , CM000683.2:g.46367030T>G	GRCh38
NC_000021.8:g.47786945T>G , CM000683.1:g.47786945T>G	GRCh37
NC_000021.7:g.46611373T>G	NCBI36
NG_008961.1:g.47910T>G
NG_008961.2:g.47909T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1552T>G	ENSP00000511987.1:n.*1552T>G
ENST00000695525.1:n.3142T>G
ENST00000695558.1:c.3056T>G	ENSP00000512015.1:p.Leu1019Arg
ENST00000703224.1:c.*2299T>G	ENSP00000515242.1:n.*2299T>G
ENST00000359568.10:c.3056T>G MANE Select	ENSP00000352572.5:p.Leu1019Arg
ENST00000359568.9:c.3056T>G	ENSP00000352572.5:p.Leu1019Arg
ENST00000480896.5:n.3325T>G
NM_001315529.1:c.2702T>G	NP_001302458.1:p.Leu901Arg
NM_006031.5:c.3056T>G	NP_006022.3:p.Leu1019Arg
XM_005261124.3:c.3056T>G	XP_005261181.1:p.Leu1019Arg
XM_011529593.1:c.3137T>G	XP_011527895.1:p.Leu1046Arg
XM_011529594.1:c.3137T>G	XP_011527896.1:p.Leu1046Arg
XM_005261124.5:c.3056T>G	XP_005261181.1:p.Leu1019Arg
XM_011529594.3:c.3137T>G	XP_011527896.1:p.Leu1046Arg
XM_017028362.2:c.3056T>G	XP_016883851.1:p.Leu1019Arg
XM_017028363.1:c.2702T>G	XP_016883852.1:p.Leu901Arg
XM_024452082.1:c.1940T>G	XP_024307850.1:p.Leu647Arg
XM_024452083.1:c.836T>G	XP_024307851.1:p.Leu279Arg
NM_006031.6:c.3056T>G MANE Select	NP_006022.3:p.Leu1019Arg
NM_001315529.2:c.2702T>G	NP_001302458.1:p.Leu901Arg