Canonical Allele Identifier: CA2260271708

Gene: CNP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41973846G= , CM000679.2:g.41973846G=	GRCh38
NC_000017.10:g.40125864G= , CM000679.1:g.40125864G=	GRCh37
NC_000017.9:g.37379390G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_033133.5:c.1188G= MANE Select	NP_149124.3:p.Gly396=
ENST00000393892.8:c.1188G= MANE Select	ENSP00000377470.2:p.Gly396=
NM_001330216.1:c.1128G=	NP_001317145.1:p.Gly376=
NM_001330216.2:c.1128G=	NP_001317145.1:p.Gly376=
NM_033133.4:c.1188G=	NP_149124.3:p.Gly396=
ENST00000393888.1:c.1128G=	ENSP00000377466.1:p.Gly376=
ENST00000393892.7:c.1188G=	ENSP00000377470.2:p.Gly396=
ENST00000472031.1:c.*365G=	ENSP00000467641.1:n.*365G=
ENST00000486438.1:n.795G=
XM_006721701.2:c.1128G=	XP_006721764.1:p.Gly376=
XM_011524340.1:c.1128G=	XP_011522642.1:p.Gly376=
XM_011524340.2:c.1128G=	XP_011522642.1:p.Gly376=