Canonical Allele Identifier: CA65960513

Gene: CNPPD1

Linked Data

• dbSNP Id: rs1043161
• MyVariant Identifiers: chr2:g.220037510C>G (hg19) ; chr2:g.219172788C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219172788C>G , CM000664.2:g.219172788C>G	GRCh38
NC_000002.11:g.220037510C>G , CM000664.1:g.220037510C>G	GRCh37
NC_000002.10:g.219745754C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360507.10:c.1031G>C MANE Select	ENSP00000353698.5:p.Arg344Thr
ENST00000360507.9:c.1031G>C	ENSP00000353698.5:p.Arg344Thr
ENST00000409789.5:c.1031G>C	ENSP00000386277.1:p.Arg344Thr
NM_015680.4:c.1031G>C	NP_056495.3:p.Arg344Thr
XM_005246462.2:c.1031G>C	XP_005246519.1:p.Arg344Thr
XM_005246463.3:c.1031G>C	XP_005246520.1:p.Arg344Thr
XM_006712419.1:c.1031G>C	XP_006712482.1:p.Arg344Thr
NM_001321389.1:c.1031G>C	NP_001308318.1:p.Arg344Thr
NM_001321390.1:c.1031G>C	NP_001308319.1:p.Arg344Thr
NM_001321391.1:c.1031G>C	NP_001308320.1:p.Arg344Thr
NM_015680.5:c.1031G>C	NP_056495.3:p.Arg344Thr
NR_135628.1:n.1076G>C
NR_135629.1:n.1134G>C
XM_024452790.1:c.1061G>C	XP_024308558.1:p.Arg354Thr
NM_015680.6:c.1031G>C MANE Select	NP_056495.4:p.Arg344Thr
NM_001321390.2:c.1031G>C	NP_001308319.2:p.Arg344Thr
NM_001321391.2:c.1031G>C	NP_001308320.2:p.Arg344Thr
NR_135628.2:n.1059G>C
NR_135629.2:n.1066G>C
NM_001321389.2:c.1031G>C	NP_001308318.2:p.Arg344Thr