Canonical Allele Identifier: CA297075869
Gene: NPC1 HGNC NCBI

Linked Data

dbSNP Id: rs372790450

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23533279_23533283del , CM000680.2:g.23533279_23533283del GRCh38
NC_000018.9:g.21113243_21113247del , CM000680.1:g.21113243_21113247del GRCh37
NC_000018.8:g.19367241_19367245del NCBI36
NG_012795.1:g.58338_58342del
NG_033119.1:g.34810_34814del

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.3754+75_3754+79del MANE Select ENSP00000269228.4:n.3754+75_3754+79del
ENST00000269228.9:c.3754+75_3754+79del ENSP00000269228.4:n.3754+75_3754+79del
ENST00000586150.5:c.509+75_509+79del
ENST00000587163.1:n.353_357del
ENST00000588867.1:n.1437+75_1437+79del
ENST00000590723.5:c.163+75_163+79del ENSP00000464755.1:n.163+75_163+79del
ENST00000591051.1:c.2832+75_2832+79del
ENST00000591107.6:c.431+75_431+79del
ENST00000593280.2:c.86+75_86+79del
NM_000271.4:c.3754+75_3754+79del NP_000262.2:n.3754+75_3754+79del
XM_005258277.1:c.3805+75_3805+79del XP_005258334.1:n.3805+75_3805+79del
XM_005258278.3:c.3805+75_3805+79del XP_005258335.1:n.3805+75_3805+79del
XM_005258279.1:c.3754+75_3754+79del XP_005258336.1:n.3754+75_3754+79del
XM_006722479.2:c.3805+75_3805+79del XP_006722542.1:n.3805+75_3805+79del
XM_011526015.1:c.3340+75_3340+79del XP_011524317.1:n.3340+75_3340+79del
XM_005258278.5:c.3805+75_3805+79del XP_005258335.1:n.3805+75_3805+79del
XM_005258279.2:c.3754+75_3754+79del XP_005258336.1:n.3754+75_3754+79del
XM_006722479.3:c.3805+75_3805+79del XP_006722542.1:n.3805+75_3805+79del
XM_017025784.1:c.3805+75_3805+79del XP_016881273.1:n.3805+75_3805+79del
XM_017025785.1:c.3805+75_3805+79del XP_016881274.1:n.3805+75_3805+79del
XM_017025786.1:c.3754+75_3754+79del XP_016881275.1:n.3754+75_3754+79del
XM_017025787.1:c.3754+75_3754+79del XP_016881276.1:n.3754+75_3754+79del
NM_000271.5:c.3754+75_3754+79del MANE Select NP_000262.2:n.3754+75_3754+79del