Canonical Allele Identifier: CA2734659380
Gene: NPC1 HGNC NCBI

Linked Data

dbSNP Id: rs2145371510

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23539594_23539596del , CM000680.2:g.23539594_23539596del GRCh38
NC_000018.9:g.21119558_21119560del , CM000680.1:g.21119558_21119560del GRCh37
NC_000018.8:g.19373556_19373558del NCBI36
NG_012795.1:g.52024_52026del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.2796-124_2796-122del MANE Select ENSP00000269228.4:n.2796-124_2796-122del
ENST00000269228.9:c.2796-124_2796-122del ENSP00000269228.4:n.2796-124_2796-122del
ENST00000591051.1:c.1874-124_1874-122del
ENST00000591075.1:n.305_307del
NM_000271.4:c.2796-124_2796-122del NP_000262.2:n.2796-124_2796-122del
XM_005258277.1:c.2847-124_2847-122del XP_005258334.1:n.2847-124_2847-122del
XM_005258278.3:c.2847-124_2847-122del XP_005258335.1:n.2847-124_2847-122del
XM_005258279.1:c.2796-124_2796-122del XP_005258336.1:n.2796-124_2796-122del
XM_006722479.2:c.2847-124_2847-122del XP_006722542.1:n.2847-124_2847-122del
XM_011526015.1:c.2382-124_2382-122del XP_011524317.1:n.2382-124_2382-122del
XM_005258278.5:c.2847-124_2847-122del XP_005258335.1:n.2847-124_2847-122del
XM_005258279.2:c.2796-124_2796-122del XP_005258336.1:n.2796-124_2796-122del
XM_006722479.3:c.2847-124_2847-122del XP_006722542.1:n.2847-124_2847-122del
XM_017025784.1:c.2847-124_2847-122del XP_016881273.1:n.2847-124_2847-122del
XM_017025785.1:c.2847-124_2847-122del XP_016881274.1:n.2847-124_2847-122del
XM_017025786.1:c.2796-124_2796-122del XP_016881275.1:n.2796-124_2796-122del
XM_017025787.1:c.2796-124_2796-122del XP_016881276.1:n.2796-124_2796-122del
NM_000271.5:c.2796-124_2796-122del MANE Select NP_000262.2:n.2796-124_2796-122del