Canonical Allele Identifier: CA322031096

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46445437G>A , CM000683.2:g.46445437G>A	GRCh38
NC_000021.8:g.47865350G>A , CM000683.1:g.47865350G>A	GRCh37
NC_000021.7:g.46689778G>A	NCBI36
NG_008961.1:g.126315G>A
NG_008961.2:g.126316G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418394.2:c.2436G>A
ENST00000695527.1:n.6447G>A
ENST00000695528.1:c.4154G>A	ENSP00000511990.1:n.4154G>A
ENST00000695529.1:n.4662G>A
ENST00000695530.1:c.2359G>A
ENST00000695531.1:n.3723G>A
ENST00000695532.1:n.3456G>A
ENST00000695533.1:n.2791G>A
ENST00000695534.1:n.3260G>A
ENST00000695535.1:n.1256G>A
ENST00000695536.1:n.1428G>A
ENST00000695537.1:n.1045G>A
ENST00000695558.1:c.*110G>A	ENSP00000512015.1:n.*110G>A
ENST00000703224.1:c.*9364G>A	ENSP00000515242.1:n.*9364G>A
ENST00000703226.1:n.2791G>A
ENST00000359568.10:c.*110G>A MANE Select	ENSP00000352572.5:n.*110G>A
ENST00000359568.9:c.*110G>A	ENSP00000352572.5:n.*110G>A
ENST00000418394.1:c.796G>A
ENST00000480896.5:n.10153G>A
NM_001315529.1:c.*110G>A	NP_001302458.1:n.*110G>A
NM_006031.5:c.*110G>A	NP_006022.3:n.*110G>A
XM_005261124.3:c.*110G>A	XP_005261181.1:n.*110G>A
XM_011529593.1:c.*110G>A	XP_011527895.1:n.*110G>A
XM_011529594.1:c.*110G>A	XP_011527896.1:n.*110G>A
XM_005261124.5:c.*110G>A	XP_005261181.1:n.*110G>A
XM_011529594.3:c.*110G>A	XP_011527896.1:n.*110G>A
XM_017028362.2:c.*110G>A	XP_016883851.1:n.*110G>A
XM_017028363.1:c.*110G>A	XP_016883852.1:n.*110G>A
XM_024452082.1:c.*110G>A	XP_024307850.1:n.*110G>A
XM_024452083.1:c.*110G>A	XP_024307851.1:n.*110G>A
NM_006031.6:c.*110G>A MANE Select	NP_006022.3:n.*110G>A
NM_001315529.2:c.*110G>A	NP_001302458.1:n.*110G>A