Canonical Allele Identifier: CA1100121069
Gene: NPSR1 HGNC NCBI
NPSR1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1787072574
gnomAD v3: 7-34778354-T-A
gnomAD v4: 7-34778354-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.34778354T>A , CM000669.2:g.34778354T>A GRCh38
NC_000007.13:g.34817966T>A , CM000669.1:g.34817966T>A GRCh37
NC_000007.12:g.34784491T>A NCBI36
NG_012185.1:g.125070T>A
NG_021366.1:g.60978A>T
NG_012185.2:g.125070T>A
NG_021366.2:g.60978A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360581.6:c.281-108T>A (NPSR1) MANE Select ENSP00000353788.1:n.281-108T>A
ENST00000359791.5:c.281-108T>A (NPSR1) ENSP00000352839.1:n.281-108T>A
ENST00000360581.5:c.281-108T>A (NPSR1) ENSP00000353788.1:n.281-108T>A
ENST00000381539.3:c.281-108T>A (NPSR1) ENSP00000370950.3:n.281-108T>A
ENST00000381542.5:c.281-49047T>A (NPSR1) ENSP00000370953.1:n.281-49047T>A
ENST00000381544.6:c.281-33416T>A (NPSR1) ENSP00000370955.2:n.281-33416T>A
ENST00000381553.7:c.281-108T>A (NPSR1) ENSP00000370965.3:n.281-108T>A
ENST00000396095.6:c.281-108T>A (NPSR1) ENSP00000379402.2:n.281-108T>A
ENST00000531252.5:c.281-141T>A (NPSR1) ENSP00000433258.1:n.281-141T>A
NM_001300933.1:c.281-141T>A (NPSR1) NP_001287862.1:n.281-141T>A
NM_001300934.1:c.281-49047T>A (NPSR1) NP_001287863.1:n.281-49047T>A
NM_001300935.1:c.281-108T>A (NPSR1) NP_001287864.1:n.281-108T>A
NM_207172.1:c.281-108T>A (NPSR1) NP_997055.1:n.281-108T>A
NM_207173.1:c.281-108T>A (NPSR1) NP_997056.1:n.281-108T>A
NR_015356.2:n.172-9914A>T (NPSR1-AS1)
NM_001300933.2:c.281-141T>A (NPSR1) NP_001287862.1:n.281-141T>A
NM_207172.2:c.281-108T>A (NPSR1) MANE Select NP_997055.1:n.281-108T>A
NM_207173.2:c.281-108T>A (NPSR1) NP_997056.1:n.281-108T>A
NM_001300934.2:c.281-49047T>A (NPSR1) NP_001287863.1:n.281-49047T>A
NM_001300935.2:c.281-108T>A (NPSR1) NP_001287864.1:n.281-108T>A