Canonical Allele Identifier: CA350650487

Gene: CNPPD1

Linked Data

• MyVariant Identifiers: chr2:g.220037549G>A (hg19) ; chr2:g.219172827G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219172827G>A , CM000664.2:g.219172827G>A	GRCh38
NC_000002.11:g.220037549G>A , CM000664.1:g.220037549G>A	GRCh37
NC_000002.10:g.219745793G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360507.10:c.992C>T MANE Select	ENSP00000353698.5:p.Thr331Ile
ENST00000360507.9:c.992C>T	ENSP00000353698.5:p.Thr331Ile
ENST00000409789.5:c.992C>T	ENSP00000386277.1:p.Thr331Ile
NM_015680.4:c.992C>T	NP_056495.3:p.Thr331Ile
XM_005246462.2:c.992C>T	XP_005246519.1:p.Thr331Ile
XM_005246463.3:c.992C>T	XP_005246520.1:p.Thr331Ile
XM_006712419.1:c.992C>T	XP_006712482.1:p.Thr331Ile
NM_001321389.1:c.992C>T	NP_001308318.1:p.Thr331Ile
NM_001321390.1:c.992C>T	NP_001308319.1:p.Thr331Ile
NM_001321391.1:c.992C>T	NP_001308320.1:p.Thr331Ile
NM_015680.5:c.992C>T	NP_056495.3:p.Thr331Ile
NR_135628.1:n.1037C>T
NR_135629.1:n.1095C>T
XM_024452790.1:c.1022C>T	XP_024308558.1:p.Thr341Ile
NM_015680.6:c.992C>T MANE Select	NP_056495.4:p.Thr331Ile
NM_001321390.2:c.992C>T	NP_001308319.2:p.Thr331Ile
NM_001321391.2:c.992C>T	NP_001308320.2:p.Thr331Ile
NR_135628.2:n.1020C>T
NR_135629.2:n.1027C>T
NM_001321389.2:c.992C>T	NP_001308318.2:p.Thr331Ile