Canonical Allele Identifier: CA1699389181

Gene: NPSR1 NPSR1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.34820377G= , CM000669.2:g.34820377G=	GRCh38
NC_000007.13:g.34859989G= , CM000669.1:g.34859989G=	GRCh37
NC_000007.12:g.34826514G=	NCBI36
NG_012185.1:g.167093G=
NG_021366.1:g.18955C=
NG_012185.2:g.167093G=
NG_021366.2:g.18955C=

Transcript Alleles

HGVS	Amino-acid Change
NM_207172.2:c.479-7024G= (NPSR1) MANE Select	NP_997055.1:n.479-7024G=
ENST00000360581.6:c.479-7024G= (NPSR1) MANE Select	ENSP00000353788.1:n.479-7024G=
NM_001300933.1:c.446-7024G= (NPSR1)	NP_001287862.1:n.446-7024G=
NM_001300933.2:c.446-7024G= (NPSR1)	NP_001287862.1:n.446-7024G=
NM_001300934.1:c.281-7024G= (NPSR1)	NP_001287863.1:n.281-7024G=
NM_001300934.2:c.281-7024G= (NPSR1)	NP_001287863.1:n.281-7024G=
NM_001300935.1:c.479-7024G= (NPSR1)	NP_001287864.1:n.479-7024G=
NM_001300935.2:c.479-7024G= (NPSR1)	NP_001287864.1:n.479-7024G=
NM_207172.1:c.479-7024G= (NPSR1)	NP_997055.1:n.479-7024G=
NM_207173.1:c.479-7024G= (NPSR1)	NP_997056.1:n.479-7024G=
NM_207173.2:c.479-7024G= (NPSR1)	NP_997056.1:n.479-7024G=
NR_015356.2:n.171+13784C= (NPSR1-AS1)
ENST00000359791.5:c.479-7024G= (NPSR1)	ENSP00000352839.1:n.479-7024G=
ENST00000360581.5:c.479-7024G= (NPSR1)	ENSP00000353788.1:n.479-7024G=
ENST00000381539.3:c.479-7024G= (NPSR1)	ENSP00000370950.3:n.479-7024G=
ENST00000381542.5:c.281-7024G= (NPSR1)	ENSP00000370953.1:n.281-7024G=
ENST00000381544.6:c.375-7024G= (NPSR1)	ENSP00000370955.2:n.375-7024G=
ENST00000396095.6:c.385-7024G= (NPSR1)	ENSP00000379402.2:n.385-7024G=
ENST00000531252.5:c.446-7024G= (NPSR1)	ENSP00000433258.1:n.446-7024G=