Canonical Allele Identifier: CA988384242
Gene: NPC1 HGNC NCBI

Linked Data

dbSNP Id: rs2058774601

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23545352_23545354del , CM000680.2:g.23545352_23545354del GRCh38
NC_000018.9:g.21125316_21125318del , CM000680.1:g.21125316_21125318del GRCh37
NC_000018.8:g.19379314_19379316del NCBI36
NG_012795.1:g.46266_46268del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.1758-203_1758-201del MANE Select ENSP00000269228.4:n.1758-203_1758-201del
ENST00000269228.9:c.1758-203_1758-201del ENSP00000269228.4:n.1758-203_1758-201del
ENST00000540608.5:n.1672-203_1672-201del
ENST00000591051.1:c.836-203_836-201del
NM_000271.4:c.1758-203_1758-201del NP_000262.2:n.1758-203_1758-201del
XM_005258277.1:c.1809-203_1809-201del XP_005258334.1:n.1809-203_1809-201del
XM_005258278.3:c.1809-203_1809-201del XP_005258335.1:n.1809-203_1809-201del
XM_005258279.1:c.1758-203_1758-201del XP_005258336.1:n.1758-203_1758-201del
XM_006722479.2:c.1809-203_1809-201del XP_006722542.1:n.1809-203_1809-201del
XM_011526015.1:c.1344-203_1344-201del XP_011524317.1:n.1344-203_1344-201del
XM_005258278.5:c.1809-203_1809-201del XP_005258335.1:n.1809-203_1809-201del
XM_005258279.2:c.1758-203_1758-201del XP_005258336.1:n.1758-203_1758-201del
XM_006722479.3:c.1809-203_1809-201del XP_006722542.1:n.1809-203_1809-201del
XM_017025784.1:c.1809-203_1809-201del XP_016881273.1:n.1809-203_1809-201del
XM_017025785.1:c.1809-203_1809-201del XP_016881274.1:n.1809-203_1809-201del
XM_017025786.1:c.1758-203_1758-201del XP_016881275.1:n.1758-203_1758-201del
XM_017025787.1:c.1758-203_1758-201del XP_016881276.1:n.1758-203_1758-201del
NM_000271.5:c.1758-203_1758-201del MANE Select NP_000262.2:n.1758-203_1758-201del