Canonical Allele Identifier: CA1699372305
Gene: NPSR1 HGNC NCBI
NPSR1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1787071116

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.34778311C>T , CM000669.2:g.34778311C>T GRCh38
NC_000007.13:g.34817923C>T , CM000669.1:g.34817923C>T GRCh37
NC_000007.12:g.34784448C>T NCBI36
NG_012185.1:g.125027C>T
NG_021366.1:g.61021G>A
NG_012185.2:g.125027C>T
NG_021366.2:g.61021G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360581.6:c.281-151C>T (NPSR1) MANE Select ENSP00000353788.1:n.281-151C>T
ENST00000359791.5:c.281-151C>T (NPSR1) ENSP00000352839.1:n.281-151C>T
ENST00000360581.5:c.281-151C>T (NPSR1) ENSP00000353788.1:n.281-151C>T
ENST00000381539.3:c.281-151C>T (NPSR1) ENSP00000370950.3:n.281-151C>T
ENST00000381542.5:c.281-49090C>T (NPSR1) ENSP00000370953.1:n.281-49090C>T
ENST00000381544.6:c.281-33459C>T (NPSR1) ENSP00000370955.2:n.281-33459C>T
ENST00000381553.7:c.281-151C>T (NPSR1) ENSP00000370965.3:n.281-151C>T
ENST00000396095.6:c.281-151C>T (NPSR1) ENSP00000379402.2:n.281-151C>T
ENST00000531252.5:c.281-184C>T (NPSR1) ENSP00000433258.1:n.281-184C>T
NM_001300933.1:c.281-184C>T (NPSR1) NP_001287862.1:n.281-184C>T
NM_001300934.1:c.281-49090C>T (NPSR1) NP_001287863.1:n.281-49090C>T
NM_001300935.1:c.281-151C>T (NPSR1) NP_001287864.1:n.281-151C>T
NM_207172.1:c.281-151C>T (NPSR1) NP_997055.1:n.281-151C>T
NM_207173.1:c.281-151C>T (NPSR1) NP_997056.1:n.281-151C>T
NR_015356.2:n.172-9871G>A (NPSR1-AS1)
NM_001300933.2:c.281-184C>T (NPSR1) NP_001287862.1:n.281-184C>T
NM_207172.2:c.281-151C>T (NPSR1) MANE Select NP_997055.1:n.281-151C>T
NM_207173.2:c.281-151C>T (NPSR1) NP_997056.1:n.281-151C>T
NM_001300934.2:c.281-49090C>T (NPSR1) NP_001287863.1:n.281-49090C>T
NM_001300935.2:c.281-151C>T (NPSR1) NP_001287864.1:n.281-151C>T