Canonical Allele Identifier: CA1699397975
Gene: NPSR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.34834426C= , CM000669.2:g.34834426C= GRCh38
NC_000007.13:g.34874038C= , CM000669.1:g.34874038C= GRCh37
NC_000007.12:g.34840563C= NCBI36
NG_012185.1:g.181142C=
NG_021366.1:g.4906G=
NG_012185.2:g.181142C=
NG_021366.2:g.4906G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360581.6:c.723C= MANE Select ENSP00000353788.1:p.Ser241=
ENST00000359791.5:c.723C= ENSP00000352839.1:p.Ser241=
ENST00000360581.5:c.723C= ENSP00000353788.1:p.Ser241=
ENST00000381539.3:c.723C= ENSP00000370950.3:p.Ser241=
ENST00000381542.5:c.525C= ENSP00000370953.1:p.Ser175=
ENST00000381544.6:c.*142C= ENSP00000370955.2:n.*142C=
ENST00000396095.6:c.*218C= ENSP00000379402.2:n.*218C=
ENST00000531252.5:c.690C= ENSP00000433258.1:p.Ser230=
NM_001300933.1:c.690C= NP_001287862.1:p.Ser230=
NM_001300934.1:c.525C= NP_001287863.1:p.Ser175=
NM_001300935.1:c.723C= NP_001287864.1:p.Ser241=
NM_207172.1:c.723C= NP_997055.1:p.Ser241=
NM_207173.1:c.723C= NP_997056.1:p.Ser241=
NM_001300933.2:c.690C= NP_001287862.1:p.Ser230=
NM_207172.2:c.723C= MANE Select NP_997055.1:p.Ser241=
NM_207173.2:c.723C= NP_997056.1:p.Ser241=
NM_001300934.2:c.525C= NP_001287863.1:p.Ser175=
NM_001300935.2:c.723C= NP_001287864.1:p.Ser241=