Canonical Allele Identifier: CA322019831

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46381756G>T , CM000683.2:g.46381756G>T	GRCh38
NC_000021.8:g.47801671G>T , CM000683.1:g.47801671G>T	GRCh37
NC_000021.7:g.46626099G>T	NCBI36
NG_008961.1:g.62636G>T
NG_008961.2:g.62635G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1724G>T	ENSP00000511987.1:n.*1724G>T
ENST00000695525.1:n.3314G>T
ENST00000695558.1:c.3228G>T	ENSP00000512015.1:p.Gln1076His
ENST00000703224.1:c.*2471G>T	ENSP00000515242.1:n.*2471G>T
ENST00000359568.10:c.3228G>T MANE Select	ENSP00000352572.5:p.Gln1076His
ENST00000359568.9:c.3228G>T	ENSP00000352572.5:p.Gln1076His
ENST00000480896.5:n.3497G>T
NM_001315529.1:c.2874G>T	NP_001302458.1:p.Gln958His
NM_006031.5:c.3228G>T	NP_006022.3:p.Gln1076His
XM_005261124.3:c.3228G>T	XP_005261181.1:p.Gln1076His
XM_011529593.1:c.3309G>T	XP_011527895.1:p.Gln1103His
XM_011529594.1:c.3309G>T	XP_011527896.1:p.Gln1103His
XM_005261124.5:c.3228G>T	XP_005261181.1:p.Gln1076His
XM_011529594.3:c.3309G>T	XP_011527896.1:p.Gln1103His
XM_017028362.2:c.3228G>T	XP_016883851.1:p.Gln1076His
XM_017028363.1:c.2874G>T	XP_016883852.1:p.Gln958His
XM_024452082.1:c.2112G>T	XP_024307850.1:p.Gln704His
XM_024452083.1:c.1008G>T	XP_024307851.1:p.Gln336His
NM_006031.6:c.3228G>T MANE Select	NP_006022.3:p.Gln1076His
NM_001315529.2:c.2874G>T	NP_001302458.1:p.Gln958His