Canonical Allele Identifier: CA10078067

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46324196A>G , CM000683.2:g.46324196A>G	GRCh38
NC_000021.8:g.47744110A>G , CM000683.1:g.47744110A>G	GRCh37
NC_000021.7:g.46568538A>G	NCBI36
NG_008961.1:g.5075A>G
NG_008961.2:g.5075A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.-33A>G	ENSP00000511987.1:n.-33A>G
ENST00000695525.1:n.54A>G
ENST00000695526.1:c.-33A>G	ENSP00000511988.1:n.-33A>G
ENST00000695558.1:c.-33A>G	ENSP00000512015.1:n.-33A>G
ENST00000703224.1:c.-33A>G	ENSP00000515242.1:n.-33A>G
ENST00000359568.10:c.-33A>G MANE Select	ENSP00000352572.5:n.-33A>G
ENST00000359568.9:c.-33A>G	ENSP00000352572.5:n.-33A>G
ENST00000490468.5:n.56A>G
NM_006031.5:c.-33A>G	NP_006022.3:n.-33A>G
XM_005261124.3:c.-33A>G	XP_005261181.1:n.-33A>G
XM_011529593.1:c.-33A>G	XP_011527895.1:n.-33A>G
XM_011529594.1:c.-33A>G	XP_011527896.1:n.-33A>G
XM_005261124.5:c.-33A>G	XP_005261181.1:n.-33A>G
XM_011529594.3:c.-33A>G	XP_011527896.1:n.-33A>G
XM_017028362.2:c.-33A>G	XP_016883851.1:n.-33A>G
XM_024452083.1:c.-2141A>G	XP_024307851.1:n.-2141A>G
NM_006031.6:c.-33A>G MANE Select	NP_006022.3:n.-33A>G