Canonical Allele Identifier: CA2290166085
Gene: NPC1 HGNC NCBI

Linked Data

dbSNP Id: rs2058693329

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23540161_23540168del , CM000680.2:g.23540161_23540168del GRCh38
NC_000018.9:g.21120125_21120132del , CM000680.1:g.21120125_21120132del GRCh37
NC_000018.8:g.19374123_19374130del NCBI36
NG_012795.1:g.51450_51457del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.2605-167_2605-160del MANE Select ENSP00000269228.4:n.2605-167_2605-160del
ENST00000269228.9:c.2605-167_2605-160del ENSP00000269228.4:n.2605-167_2605-160del
ENST00000540608.5:n.2519-167_2519-160del
ENST00000586718.1:n.396-167_396-160del
ENST00000591051.1:c.1683-167_1683-160del
NM_000271.4:c.2605-167_2605-160del NP_000262.2:n.2605-167_2605-160del
XM_005258277.1:c.2656-167_2656-160del XP_005258334.1:n.2656-167_2656-160del
XM_005258278.3:c.2656-167_2656-160del XP_005258335.1:n.2656-167_2656-160del
XM_005258279.1:c.2605-167_2605-160del XP_005258336.1:n.2605-167_2605-160del
XM_006722479.2:c.2656-167_2656-160del XP_006722542.1:n.2656-167_2656-160del
XM_011526015.1:c.2191-167_2191-160del XP_011524317.1:n.2191-167_2191-160del
XM_005258278.5:c.2656-167_2656-160del XP_005258335.1:n.2656-167_2656-160del
XM_005258279.2:c.2605-167_2605-160del XP_005258336.1:n.2605-167_2605-160del
XM_006722479.3:c.2656-167_2656-160del XP_006722542.1:n.2656-167_2656-160del
XM_017025784.1:c.2656-167_2656-160del XP_016881273.1:n.2656-167_2656-160del
XM_017025785.1:c.2656-167_2656-160del XP_016881274.1:n.2656-167_2656-160del
XM_017025786.1:c.2605-167_2605-160del XP_016881275.1:n.2605-167_2605-160del
XM_017025787.1:c.2605-167_2605-160del XP_016881276.1:n.2605-167_2605-160del
NM_000271.5:c.2605-167_2605-160del MANE Select NP_000262.2:n.2605-167_2605-160del