Canonical Allele Identifier: CA367260462
Gene: NPSR1 HGNC NCBI
NPSR1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.34778512A>C , CM000669.2:g.34778512A>C GRCh38
NC_000007.13:g.34818124A>C , CM000669.1:g.34818124A>C GRCh37
NC_000007.12:g.34784649A>C NCBI36
NG_012185.1:g.125228A>C
NG_021366.1:g.60820T>G
NG_012185.2:g.125228A>C
NG_021366.2:g.60820T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360581.6:c.331A>C (NPSR1) MANE Select ENSP00000353788.1:p.Thr111Pro
ENST00000359791.5:c.331A>C (NPSR1) ENSP00000352839.1:p.Thr111Pro
ENST00000360581.5:c.331A>C (NPSR1) ENSP00000353788.1:p.Thr111Pro
ENST00000381539.3:c.331A>C (NPSR1) ENSP00000370950.3:p.Thr111Pro
ENST00000381542.5:c.281-48889A>C (NPSR1) ENSP00000370953.1:n.281-48889A>C
ENST00000381544.6:c.281-33258A>C (NPSR1) ENSP00000370955.2:n.281-33258A>C
ENST00000381553.7:c.331A>C (NPSR1) ENSP00000370965.3:p.Thr111Pro
ENST00000396095.6:c.331A>C (NPSR1) ENSP00000379402.2:p.Thr111Pro
ENST00000531252.5:c.298A>C (NPSR1) ENSP00000433258.1:p.Thr100Pro
NM_001300933.1:c.298A>C (NPSR1) NP_001287862.1:p.Thr100Pro
NM_001300934.1:c.281-48889A>C (NPSR1) NP_001287863.1:n.281-48889A>C
NM_001300935.1:c.331A>C (NPSR1) NP_001287864.1:p.Thr111Pro
NM_207172.1:c.331A>C (NPSR1) NP_997055.1:p.Thr111Pro
NM_207173.1:c.331A>C (NPSR1) NP_997056.1:p.Thr111Pro
NR_015356.2:n.172-10072T>G (NPSR1-AS1)
NM_001300933.2:c.298A>C (NPSR1) NP_001287862.1:p.Thr100Pro
NM_207172.2:c.331A>C (NPSR1) MANE Select NP_997055.1:p.Thr111Pro
NM_207173.2:c.331A>C (NPSR1) NP_997056.1:p.Thr111Pro
NM_001300934.2:c.281-48889A>C (NPSR1) NP_001287863.1:n.281-48889A>C
NM_001300935.2:c.331A>C (NPSR1) NP_001287864.1:p.Thr111Pro