Canonical Allele Identifier: CA431420895

Gene: CNPPD1

Linked Data

• gnomAD v4: 2-219172826-A-C
• MyVariant Identifiers: chr2:g.220037548A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219172826A>C , CM000664.2:g.219172826A>C	GRCh38
NC_000002.11:g.220037548A>C , CM000664.1:g.220037548A>C	GRCh37
NC_000002.10:g.219745792A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360507.10:c.993T>G MANE Select	ENSP00000353698.5:p.Thr331=
ENST00000360507.9:c.993T>G	ENSP00000353698.5:p.Thr331=
ENST00000409789.5:c.993T>G	ENSP00000386277.1:p.Thr331=
NM_015680.4:c.993T>G	NP_056495.3:p.Thr331=
XM_005246462.2:c.993T>G	XP_005246519.1:p.Thr331=
XM_005246463.3:c.993T>G	XP_005246520.1:p.Thr331=
XM_006712419.1:c.993T>G	XP_006712482.1:p.Thr331=
NM_001321389.1:c.993T>G	NP_001308318.1:p.Thr331=
NM_001321390.1:c.993T>G	NP_001308319.1:p.Thr331=
NM_001321391.1:c.993T>G	NP_001308320.1:p.Thr331=
NM_015680.5:c.993T>G	NP_056495.3:p.Thr331=
NR_135628.1:n.1038T>G
NR_135629.1:n.1096T>G
XM_024452790.1:c.1023T>G	XP_024308558.1:p.Thr341=
NM_015680.6:c.993T>G MANE Select	NP_056495.4:p.Thr331=
NM_001321390.2:c.993T>G	NP_001308319.2:p.Thr331=
NM_001321391.2:c.993T>G	NP_001308320.2:p.Thr331=
NR_135628.2:n.1021T>G
NR_135629.2:n.1028T>G
NM_001321389.2:c.993T>G	NP_001308318.2:p.Thr331=