Canonical Allele Identifier: CA431420742

Gene: CNPPD1

Linked Data

• MyVariant Identifiers: chr2:g.220037785T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219173063T>G , CM000664.2:g.219173063T>G	GRCh38
NC_000002.11:g.220037785T>G , CM000664.1:g.220037785T>G	GRCh37
NC_000002.10:g.219746029T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360507.10:c.756A>C MANE Select	ENSP00000353698.5:p.Val252=
ENST00000360507.9:c.756A>C	ENSP00000353698.5:p.Val252=
ENST00000409789.5:c.756A>C	ENSP00000386277.1:p.Val252=
ENST00000451647.1:c.837A>C	ENSP00000405997.1:p.Val279=
ENST00000453038.5:c.756A>C	ENSP00000410109.1:p.Val252=
NM_015680.4:c.756A>C	NP_056495.3:p.Val252=
XM_005246462.2:c.756A>C	XP_005246519.1:p.Val252=
XM_005246463.3:c.756A>C	XP_005246520.1:p.Val252=
XM_006712419.1:c.756A>C	XP_006712482.1:p.Val252=
NM_001321389.1:c.756A>C	NP_001308318.1:p.Val252=
NM_001321390.1:c.756A>C	NP_001308319.1:p.Val252=
NM_001321391.1:c.756A>C	NP_001308320.1:p.Val252=
NM_015680.5:c.756A>C	NP_056495.3:p.Val252=
NR_135628.1:n.801A>C
NR_135629.1:n.859A>C
XM_024452790.1:c.786A>C	XP_024308558.1:p.Val262=
NM_015680.6:c.756A>C MANE Select	NP_056495.4:p.Val252=
NM_001321390.2:c.756A>C	NP_001308319.2:p.Val252=
NM_001321391.2:c.756A>C	NP_001308320.2:p.Val252=
NR_135628.2:n.784A>C
NR_135629.2:n.791A>C
NM_001321389.2:c.756A>C	NP_001308318.2:p.Val252=