Canonical Allele Identifier: CA1537662608

Gene: NPR3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32768573_32768574delinsTG , CM000667.2:g.32768573_32768574delinsTG	GRCh38
NC_000005.9:g.32768679_32768680delinsTG , CM000667.1:g.32768679_32768680delinsTG	GRCh37
NC_000005.8:g.32804436_32804437delinsTG	NCBI36
NG_028162.1:g.62937_62938delinsTG
NG_028162.2:g.84498_84499delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000265074.13:c.1060-6135_1060-6134delinsTG MANE Select	ENSP00000265074.8:n.1060-6135_1060-6134de...
ENST00000265074.12:c.1060-6135_1060-6134delinsTG	ENSP00000265074.8:n.1060-6135_1060-6134de...
ENST00000326958.5:c.412-6135_412-6134delinsTG	ENSP00000318340.2:n.412-6135_412-6134deli...
ENST00000415167.2:c.1060-6135_1060-6134delinsTG	ENSP00000398028.2:n.1060-6135_1060-6134de...
ENST00000434067.6:c.412-6135_412-6134delinsTG	ENSP00000388408.2:n.412-6135_412-6134deli...
ENST00000506712.1:n.421-6135_421-6134delinsTG
ENST00000509104.5:c.391-6135_391-6134delinsTG	ENSP00000425325.1:n.391-6135_391-6134deli...
NM_000908.3:c.1060-6135_1060-6134delinsTG	NP_000899.1:n.1060-6135_1060-6134delinsTG...
NM_001204375.1:c.1060-6135_1060-6134delinsTG	NP_001191304.1:n.1060-6135_1060-6134delin...
NM_001204376.1:c.412-6135_412-6134delinsTG	NP_001191305.1:n.412-6135_412-6134delinsT...
XM_005248309.1:c.412-6135_412-6134delinsTG	XP_005248366.1:n.412-6135_412-6134delinsT...
XM_011514047.1:c.391-6135_391-6134delinsTG	XP_011512349.1:n.391-6135_391-6134delinsT...
XM_011514048.1:c.340-6135_340-6134delinsTG	XP_011512350.1:n.340-6135_340-6134delinsT...
XM_011514049.1:c.283-6135_283-6134delinsTG	XP_011512351.1:n.283-6135_283-6134delinsT...
NM_001363652.1:c.412-6135_412-6134delinsTG	NP_001350581.1:n.412-6135_412-6134delinsT...
NM_001364458.1:c.340-6135_340-6134delinsTG	NP_001351387.1:n.340-6135_340-6134delinsT...
NM_001364460.1:c.289-6135_289-6134delinsTG	NP_001351389.1:n.289-6135_289-6134delinsT...
XM_011514047.2:c.391-6135_391-6134delinsTG	XP_011512349.1:n.391-6135_391-6134delinsT...
XM_011514049.3:c.283-6135_283-6134delinsTG	XP_011512351.1:n.283-6135_283-6134delinsT...
XM_017009492.2:c.937-6135_937-6134delinsTG	XP_016864981.1:n.937-6135_937-6134delinsT...
NM_001204375.2:c.1060-6135_1060-6134delinsTG MANE Select	NP_001191304.1:n.1060-6135_1060-6134delin...
NM_000908.4:c.1060-6135_1060-6134delinsTG	NP_000899.1:n.1060-6135_1060-6134delinsTG...
NM_001363652.2:c.412-6135_412-6134delinsTG	NP_001350581.1:n.412-6135_412-6134delinsT...
NM_001364458.2:c.340-6135_340-6134delinsTG	NP_001351387.1:n.340-6135_340-6134delinsT...
NM_001364460.2:c.289-6135_289-6134delinsTG	NP_001351389.1:n.289-6135_289-6134delinsT...
NM_001204376.2:c.412-6135_412-6134delinsTG	NP_001191305.1:n.412-6135_412-6134delinsT...