Canonical Allele Identifier: CA1329092313

Gene: CNPPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219173077C= , CM000664.2:g.219173077C=	GRCh38
NC_000002.11:g.220037799C= , CM000664.1:g.220037799C=	GRCh37
NC_000002.10:g.219746043C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360507.10:c.742G= MANE Select	ENSP00000353698.5:p.Ala248=
ENST00000360507.9:c.742G=	ENSP00000353698.5:p.Ala248=
ENST00000409789.5:c.742G=	ENSP00000386277.1:p.Ala248=
ENST00000451647.1:c.823G=	ENSP00000405997.1:p.Ala275=
ENST00000453038.5:c.742G=	ENSP00000410109.1:p.Ala248=
NM_015680.4:c.742G=	NP_056495.3:p.Ala248=
XM_005246462.2:c.742G=	XP_005246519.1:p.Ala248=
XM_005246463.3:c.742G=	XP_005246520.1:p.Ala248=
XM_006712419.1:c.742G=	XP_006712482.1:p.Ala248=
NM_001321389.1:c.742G=	NP_001308318.1:p.Ala248=
NM_001321390.1:c.742G=	NP_001308319.1:p.Ala248=
NM_001321391.1:c.742G=	NP_001308320.1:p.Ala248=
NM_015680.5:c.742G=	NP_056495.3:p.Ala248=
NR_135628.1:n.787G=
NR_135629.1:n.845G=
XM_024452790.1:c.772G=	XP_024308558.1:p.Ala258=
NM_015680.6:c.742G= MANE Select	NP_056495.4:p.Ala248=
NM_001321390.2:c.742G=	NP_001308319.2:p.Ala248=
NM_001321391.2:c.742G=	NP_001308320.2:p.Ala248=
NR_135628.2:n.770G=
NR_135629.2:n.777G=
NM_001321389.2:c.742G=	NP_001308318.2:p.Ala248=