Canonical Allele Identifier: CA410569865

Gene: PCNT

Linked Data

• MyVariant Identifiers: chr21:g.47786889A>C (hg19) ; chr21:g.46366974A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46366974A>C , CM000683.2:g.46366974A>C	GRCh38
NC_000021.8:g.47786889A>C , CM000683.1:g.47786889A>C	GRCh37
NC_000021.7:g.46611317A>C	NCBI36
NG_008961.1:g.47854A>C
NG_008961.2:g.47853A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1496A>C	ENSP00000511987.1:n.*1496A>C
ENST00000695525.1:n.3086A>C
ENST00000695558.1:c.3000A>C	ENSP00000512015.1:p.Gln1000His
ENST00000703224.1:c.*2243A>C	ENSP00000515242.1:n.*2243A>C
ENST00000359568.10:c.3000A>C MANE Select	ENSP00000352572.5:p.Gln1000His
ENST00000359568.9:c.3000A>C	ENSP00000352572.5:p.Gln1000His
ENST00000480896.5:n.3269A>C
NM_001315529.1:c.2646A>C	NP_001302458.1:p.Gln882His
NM_006031.5:c.3000A>C	NP_006022.3:p.Gln1000His
XM_005261124.3:c.3000A>C	XP_005261181.1:p.Gln1000His
XM_011529593.1:c.3081A>C	XP_011527895.1:p.Gln1027His
XM_011529594.1:c.3081A>C	XP_011527896.1:p.Gln1027His
XM_005261124.5:c.3000A>C	XP_005261181.1:p.Gln1000His
XM_011529594.3:c.3081A>C	XP_011527896.1:p.Gln1027His
XM_017028362.2:c.3000A>C	XP_016883851.1:p.Gln1000His
XM_017028363.1:c.2646A>C	XP_016883852.1:p.Gln882His
XM_024452082.1:c.1884A>C	XP_024307850.1:p.Gln628His
XM_024452083.1:c.780A>C	XP_024307851.1:p.Gln260His
NM_006031.6:c.3000A>C MANE Select	NP_006022.3:p.Gln1000His
NM_001315529.2:c.2646A>C	NP_001302458.1:p.Gln882His