Canonical Allele Identifier: CA512734527

Gene: PCNT

Linked Data

• MyVariant Identifiers: chr21:g.47787009A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46367094A>C , CM000683.2:g.46367094A>C	GRCh38
NC_000021.8:g.47787009A>C , CM000683.1:g.47787009A>C	GRCh37
NC_000021.7:g.46611437A>C	NCBI36
NG_008961.1:g.47974A>C
NG_008961.2:g.47973A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466474.6:c.*1616A>C	ENSP00000511987.1:n.*1616A>C
ENST00000695525.1:n.3206A>C
ENST00000695558.1:c.3120A>C	ENSP00000512015.1:p.Thr1040=
ENST00000703224.1:c.*2363A>C	ENSP00000515242.1:n.*2363A>C
ENST00000359568.10:c.3120A>C MANE Select	ENSP00000352572.5:p.Thr1040=
ENST00000359568.9:c.3120A>C	ENSP00000352572.5:p.Thr1040=
ENST00000480896.5:n.3389A>C
NM_001315529.1:c.2766A>C	NP_001302458.1:p.Thr922=
NM_006031.5:c.3120A>C	NP_006022.3:p.Thr1040=
XM_005261124.3:c.3120A>C	XP_005261181.1:p.Thr1040=
XM_011529593.1:c.3201A>C	XP_011527895.1:p.Thr1067=
XM_011529594.1:c.3201A>C	XP_011527896.1:p.Thr1067=
XM_005261124.5:c.3120A>C	XP_005261181.1:p.Thr1040=
XM_011529594.3:c.3201A>C	XP_011527896.1:p.Thr1067=
XM_017028362.2:c.3120A>C	XP_016883851.1:p.Thr1040=
XM_017028363.1:c.2766A>C	XP_016883852.1:p.Thr922=
XM_024452082.1:c.2004A>C	XP_024307850.1:p.Thr668=
XM_024452083.1:c.900A>C	XP_024307851.1:p.Thr300=
NM_006031.6:c.3120A>C MANE Select	NP_006022.3:p.Thr1040=
NM_001315529.2:c.2766A>C	NP_001302458.1:p.Thr922=