Canonical Allele Identifier: CA2758454240

Gene: NPHP3 NPHP3-ACAD11

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.132689414_132689417del , CM000665.2:g.132689414_132689417del	GRCh38
NC_000003.11:g.132408258_132408261del , CM000665.1:g.132408258_132408261del	GRCh37
NC_000003.10:g.133890948_133890951del	NCBI36
NG_008130.1:g.38016_38019del
NG_008130.2:g.38016_38019del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684294.1:c.*602-154_*602-151del (NPHP3)	ENSP00000508078.1:n.*602-154_*602-151del
ENST00000337331.10:c.2694-154_2694-151del (NPHP3) MANE Select	ENSP00000338766.5:n.2694-154_2694-151del
ENST00000337331.9:c.2694-154_2694-151del (NPHP3)	ENSP00000338766.5:n.2694-154_2694-151del
ENST00000465756.5:c.*602-154_*602-151del (NPHP3)	ENSP00000419907.1:n.*602-154_*602-151del
ENST00000471702.2:c.*685-154_*685-151del (NPHP3-ACAD11)	ENSP00000419763.1:n.*685-154_*685-151del
ENST00000474871.5:n.428-154_428-151del (NPHP3)
ENST00000490993.5:n.3419-154_3419-151del (NPHP3)
NM_153240.4:c.2694-154_2694-151del (NPHP3)	NP_694972.3:n.2694-154_2694-151del
NR_037804.1:n.2700-154_2700-151del (NPHP3-ACAD11)
NM_153240.5:c.2694-154_2694-151del (NPHP3) MANE Select	NP_694972.3:n.2694-154_2694-151del