Canonical Allele Identifier: CA1100121063
Gene: NPSR1 HGNC NCBI
NPSR1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1787071429
gnomAD v3: 7-34778319-C-A
gnomAD v4: 7-34778319-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.34778319C>A , CM000669.2:g.34778319C>A GRCh38
NC_000007.13:g.34817931C>A , CM000669.1:g.34817931C>A GRCh37
NC_000007.12:g.34784456C>A NCBI36
NG_012185.1:g.125035C>A
NG_021366.1:g.61013G>T
NG_012185.2:g.125035C>A
NG_021366.2:g.61013G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360581.6:c.281-143C>A (NPSR1) MANE Select ENSP00000353788.1:n.281-143C>A
ENST00000359791.5:c.281-143C>A (NPSR1) ENSP00000352839.1:n.281-143C>A
ENST00000360581.5:c.281-143C>A (NPSR1) ENSP00000353788.1:n.281-143C>A
ENST00000381539.3:c.281-143C>A (NPSR1) ENSP00000370950.3:n.281-143C>A
ENST00000381542.5:c.281-49082C>A (NPSR1) ENSP00000370953.1:n.281-49082C>A
ENST00000381544.6:c.281-33451C>A (NPSR1) ENSP00000370955.2:n.281-33451C>A
ENST00000381553.7:c.281-143C>A (NPSR1) ENSP00000370965.3:n.281-143C>A
ENST00000396095.6:c.281-143C>A (NPSR1) ENSP00000379402.2:n.281-143C>A
ENST00000531252.5:c.281-176C>A (NPSR1) ENSP00000433258.1:n.281-176C>A
NM_001300933.1:c.281-176C>A (NPSR1) NP_001287862.1:n.281-176C>A
NM_001300934.1:c.281-49082C>A (NPSR1) NP_001287863.1:n.281-49082C>A
NM_001300935.1:c.281-143C>A (NPSR1) NP_001287864.1:n.281-143C>A
NM_207172.1:c.281-143C>A (NPSR1) NP_997055.1:n.281-143C>A
NM_207173.1:c.281-143C>A (NPSR1) NP_997056.1:n.281-143C>A
NR_015356.2:n.172-9879G>T (NPSR1-AS1)
NM_001300933.2:c.281-176C>A (NPSR1) NP_001287862.1:n.281-176C>A
NM_207172.2:c.281-143C>A (NPSR1) MANE Select NP_997055.1:n.281-143C>A
NM_207173.2:c.281-143C>A (NPSR1) NP_997056.1:n.281-143C>A
NM_001300934.2:c.281-49082C>A (NPSR1) NP_001287863.1:n.281-49082C>A
NM_001300935.2:c.281-143C>A (NPSR1) NP_001287864.1:n.281-143C>A