Canonical Allele Identifier: CA1699394844
Gene: NPSR1 HGNC NCBI
NPSR1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.34827538T= , CM000669.2:g.34827538T= GRCh38
NC_000007.13:g.34867150T= , CM000669.1:g.34867150T= GRCh37
NC_000007.12:g.34833675T= NCBI36
NG_012185.1:g.174254T=
NG_021366.1:g.11794A=
NG_012185.2:g.174254T=
NG_021366.2:g.11794A=

Transcript Alleles

HGVS Amino-acid Change
NM_207172.2:c.616T= (NPSR1) MANE Select NP_997055.1:p.Tyr206=
ENST00000360581.6:c.616T= (NPSR1) MANE Select ENSP00000353788.1:p.Tyr206=
NM_001300933.1:c.583T= (NPSR1) NP_001287862.1:p.Tyr195=
NM_001300933.2:c.583T= (NPSR1) NP_001287862.1:p.Tyr195=
NM_001300934.1:c.418T= (NPSR1) NP_001287863.1:p.Tyr140=
NM_001300934.2:c.418T= (NPSR1) NP_001287863.1:p.Tyr140=
NM_001300935.1:c.616T= (NPSR1) NP_001287864.1:p.Tyr206=
NM_001300935.2:c.616T= (NPSR1) NP_001287864.1:p.Tyr206=
NM_207172.1:c.616T= (NPSR1) NP_997055.1:p.Tyr206=
NM_207173.1:c.616T= (NPSR1) NP_997056.1:p.Tyr206=
NM_207173.2:c.616T= (NPSR1) NP_997056.1:p.Tyr206=
NR_015356.2:n.171+6623A= (NPSR1-AS1)
ENST00000359791.5:c.616T= (NPSR1) ENSP00000352839.1:p.Tyr206=
ENST00000360581.5:c.616T= (NPSR1) ENSP00000353788.1:p.Tyr206=
ENST00000381539.3:c.616T= (NPSR1) ENSP00000370950.3:p.Tyr206=
ENST00000381542.5:c.418T= (NPSR1) ENSP00000370953.1:p.Tyr140=
ENST00000381544.6:c.*35T= (NPSR1) ENSP00000370955.2:n.*35T=
ENST00000396095.6:c.*111T= (NPSR1) ENSP00000379402.2:n.*111T=
ENST00000531252.5:c.583T= (NPSR1) ENSP00000433258.1:p.Tyr195=