Canonical Allele Identifier: CA1699404460

Gene: NPSR1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.34849570A= , CM000669.2:g.34849570A=	GRCh38
NC_000007.13:g.34889182A= , CM000669.1:g.34889182A=	GRCh37
NC_000007.12:g.34855707A=	NCBI36
NG_012185.1:g.196286A=
NG_012185.2:g.196286A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360581.6:c.1031A= MANE Select	ENSP00000353788.1:p.Gln344=
ENST00000359791.5:c.1025+907A=	ENSP00000352839.1:n.1025+907A=
ENST00000360581.5:c.1031A=	ENSP00000353788.1:p.Gln344=
ENST00000381539.3:c.1131A=	ENSP00000370950.3:p.Ala377=
ENST00000381542.5:c.833A=	ENSP00000370953.1:p.Gln278=
ENST00000381544.6:c.*450A=	ENSP00000370955.2:n.*450A=
ENST00000396095.6:c.*526A=	ENSP00000379402.2:n.*526A=
ENST00000531252.5:c.992+907A=	ENSP00000433258.1:n.992+907A=
NM_001300933.1:c.992+907A=	NP_001287862.1:n.992+907A=
NM_001300934.1:c.833A=	NP_001287863.1:p.Gln278=
NM_001300935.1:c.1131A=	NP_001287864.1:p.Ala377=
NM_207172.1:c.1031A=	NP_997055.1:p.Gln344=
NM_207173.1:c.1025+907A=	NP_997056.1:n.1025+907A=
NM_001300933.2:c.992+907A=	NP_001287862.1:n.992+907A=
NM_207172.2:c.1031A= MANE Select	NP_997055.1:p.Gln344=
NM_207173.2:c.1025+907A=	NP_997056.1:n.1025+907A=
NM_001300934.2:c.833A=	NP_001287863.1:p.Gln278=
NM_001300935.2:c.1131A=	NP_001287864.1:p.Ala377=