Canonical Allele Identifier: CA809925061
Gene: NPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1169995574

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32748487del , CM000667.2:g.32748487del GRCh38
NC_000005.9:g.32748593del , CM000667.1:g.32748593del GRCh37
NC_000005.8:g.32784350del NCBI36
NG_028162.1:g.42851del
NG_028162.2:g.64412del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265074.13:c.1059+9457del MANE Select ENSP00000265074.8:n.1059+9457del
ENST00000265074.12:c.1059+9457del ENSP00000265074.8:n.1059+9457del
ENST00000326958.5:c.411+9457del ENSP00000318340.2:n.411+9457del
ENST00000415167.2:c.1059+9457del ENSP00000398028.2:n.1059+9457del
ENST00000434067.6:c.411+9457del ENSP00000388408.2:n.411+9457del
ENST00000506712.1:n.420+9457del
ENST00000509104.5:c.390+9457del ENSP00000425325.1:n.390+9457del
NM_000908.3:c.1059+9457del NP_000899.1:n.1059+9457del
NM_001204375.1:c.1059+9457del NP_001191304.1:n.1059+9457del
NM_001204376.1:c.411+9457del NP_001191305.1:n.411+9457del
XM_005248309.1:c.411+9457del XP_005248366.1:n.411+9457del
XM_011514047.1:c.390+9457del XP_011512349.1:n.390+9457del
XM_011514048.1:c.339+9457del XP_011512350.1:n.339+9457del
XM_011514049.1:c.282+9457del XP_011512351.1:n.282+9457del
NM_001363652.1:c.411+9457del NP_001350581.1:n.411+9457del
NM_001364458.1:c.339+9457del NP_001351387.1:n.339+9457del
NM_001364460.1:c.288+9457del NP_001351389.1:n.288+9457del
XM_011514047.2:c.390+9457del XP_011512349.1:n.390+9457del
XM_011514049.3:c.282+9457del XP_011512351.1:n.282+9457del
XM_017009492.2:c.936+9457del XP_016864981.1:n.936+9457del
NM_001204375.2:c.1059+9457del MANE Select NP_001191304.1:n.1059+9457del
NM_000908.4:c.1059+9457del NP_000899.1:n.1059+9457del
NM_001363652.2:c.411+9457del NP_001350581.1:n.411+9457del
NM_001364458.2:c.339+9457del NP_001351387.1:n.339+9457del
NM_001364460.2:c.288+9457del NP_001351389.1:n.288+9457del
NM_001204376.2:c.411+9457del NP_001191305.1:n.411+9457del