Canonical Allele Identifier: CA2758454126

Gene: NPHP3 NPHP3-ACAD11

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132689302_132689315del , CM000665.2:g.132689302_132689315del	GRCh38
NC_000003.11:g.132408146_132408159del , CM000665.1:g.132408146_132408159del	GRCh37
NC_000003.10:g.133890836_133890849del	NCBI36
NG_008130.1:g.38118_38131del
NG_008130.2:g.38118_38131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684294.1:c.*602-52_*602-39del (NPHP3)	ENSP00000508078.1:n.*602-52_*602-39del
ENST00000337331.10:c.2694-52_2694-39del (NPHP3) MANE Select	ENSP00000338766.5:n.2694-52_2694-39del
ENST00000337331.9:c.2694-52_2694-39del (NPHP3)	ENSP00000338766.5:n.2694-52_2694-39del
ENST00000465756.5:c.*602-52_*602-39del (NPHP3)	ENSP00000419907.1:n.*602-52_*602-39del
ENST00000471702.2:c.*685-52_*685-39del (NPHP3-ACAD11)	ENSP00000419763.1:n.*685-52_*685-39del
ENST00000474871.5:n.428-52_428-39del (NPHP3)
ENST00000490993.5:n.3419-52_3419-39del (NPHP3)
NM_153240.4:c.2694-52_2694-39del (NPHP3)	NP_694972.3:n.2694-52_2694-39del
NR_037804.1:n.2700-52_2700-39del (NPHP3-ACAD11)
NM_153240.5:c.2694-52_2694-39del (NPHP3) MANE Select	NP_694972.3:n.2694-52_2694-39del