Canonical Allele Identifier: CA2392676544

Gene: PCNT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46431839A= , CM000683.2:g.46431839A=	GRCh38
NC_000021.8:g.47851753A= , CM000683.1:g.47851753A=	GRCh37
NC_000021.7:g.46676181A=	NCBI36
NG_008961.1:g.112718A=
NG_008961.2:g.112718A=

Transcript Alleles

HGVS	Amino-acid Change
NM_006031.6:c.8375A= MANE Select	NP_006022.3:p.Gln2792=
ENST00000359568.10:c.8375A= MANE Select	ENSP00000352572.5:p.Gln2792=
NM_001315529.1:c.8021A=	NP_001302458.1:p.Gln2674=
NM_001315529.2:c.8021A=	NP_001302458.1:p.Gln2674=
NM_006031.5:c.8375A=	NP_006022.3:p.Gln2792=
ENST00000359568.9:c.8375A=	ENSP00000352572.5:p.Gln2792=
ENST00000418394.2:c.1194A=
ENST00000480896.5:n.8644A=
ENST00000482575.1:n.382A=
ENST00000695527.1:n.2720A=
ENST00000695528.1:c.2408A=	ENSP00000511990.1:p.Gln803=
ENST00000695529.1:n.2408A=
ENST00000695530.1:c.1194A=
ENST00000695531.1:n.1977A=
ENST00000695532.1:n.1977A=
ENST00000695533.1:n.1045A=
ENST00000695534.1:n.1006A=
ENST00000695558.1:c.8408A=	ENSP00000512015.1:p.Gln2803=
ENST00000703224.1:c.*7618A=	ENSP00000515242.1:n.*7618A=
ENST00000703226.1:n.1045A=
XM_005261124.3:c.8408A=	XP_005261181.1:p.Gln2803=
XM_005261124.5:c.8408A=	XP_005261181.1:p.Gln2803=
XM_011529593.1:c.8486A=	XP_011527895.1:p.Gln2829=
XM_011529594.1:c.8456A=	XP_011527896.1:p.Gln2819=
XM_011529594.3:c.8456A=	XP_011527896.1:p.Gln2819=
XM_017028362.2:c.8375A=	XP_016883851.1:p.Gln2792=
XM_017028363.1:c.8054A=	XP_016883852.1:p.Gln2685=
XM_024452082.1:c.7292A=	XP_024307850.1:p.Gln2431=
XM_024452083.1:c.6188A=	XP_024307851.1:p.Gln2063=