Canonical Allele Identifier: CA350650556

Gene: CNPPD1

Linked Data

• MyVariant Identifiers: chr2:g.220037562G>T (hg19) ; chr2:g.219172840G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219172840G>T , CM000664.2:g.219172840G>T	GRCh38
NC_000002.11:g.220037562G>T , CM000664.1:g.220037562G>T	GRCh37
NC_000002.10:g.219745806G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360507.10:c.979C>A MANE Select	ENSP00000353698.5:p.Pro327Thr
ENST00000360507.9:c.979C>A	ENSP00000353698.5:p.Pro327Thr
ENST00000409789.5:c.979C>A	ENSP00000386277.1:p.Pro327Thr
NM_015680.4:c.979C>A	NP_056495.3:p.Pro327Thr
XM_005246462.2:c.979C>A	XP_005246519.1:p.Pro327Thr
XM_005246463.3:c.979C>A	XP_005246520.1:p.Pro327Thr
XM_006712419.1:c.979C>A	XP_006712482.1:p.Pro327Thr
NM_001321389.1:c.979C>A	NP_001308318.1:p.Pro327Thr
NM_001321390.1:c.979C>A	NP_001308319.1:p.Pro327Thr
NM_001321391.1:c.979C>A	NP_001308320.1:p.Pro327Thr
NM_015680.5:c.979C>A	NP_056495.3:p.Pro327Thr
NR_135628.1:n.1024C>A
NR_135629.1:n.1082C>A
XM_024452790.1:c.1009C>A	XP_024308558.1:p.Pro337Thr
NM_015680.6:c.979C>A MANE Select	NP_056495.4:p.Pro327Thr
NM_001321390.2:c.979C>A	NP_001308319.2:p.Pro327Thr
NM_001321391.2:c.979C>A	NP_001308320.2:p.Pro327Thr
NR_135628.2:n.1007C>A
NR_135629.2:n.1014C>A
NM_001321389.2:c.979C>A	NP_001308318.2:p.Pro327Thr