Canonical Allele Identifier: CA2290168543

Gene: NPC1

Linked Data

• dbSNP Id: rs2058774864

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23545378del , CM000680.2:g.23545378del	GRCh38
NC_000018.9:g.21125342del , CM000680.1:g.21125342del	GRCh37
NC_000018.8:g.19379340del	NCBI36
NG_012795.1:g.46242del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.1758-227del MANE Select	ENSP00000269228.4:n.1758-227del
ENST00000269228.9:c.1758-227del	ENSP00000269228.4:n.1758-227del
ENST00000540608.5:n.1672-227del
ENST00000591051.1:c.836-227del
NM_000271.4:c.1758-227del	NP_000262.2:n.1758-227del
XM_005258277.1:c.1809-227del	XP_005258334.1:n.1809-227del
XM_005258278.3:c.1809-227del	XP_005258335.1:n.1809-227del
XM_005258279.1:c.1758-227del	XP_005258336.1:n.1758-227del
XM_006722479.2:c.1809-227del	XP_006722542.1:n.1809-227del
XM_011526015.1:c.1344-227del	XP_011524317.1:n.1344-227del
XM_005258278.5:c.1809-227del	XP_005258335.1:n.1809-227del
XM_005258279.2:c.1758-227del	XP_005258336.1:n.1758-227del
XM_006722479.3:c.1809-227del	XP_006722542.1:n.1809-227del
XM_017025784.1:c.1809-227del	XP_016881273.1:n.1809-227del
XM_017025785.1:c.1809-227del	XP_016881274.1:n.1809-227del
XM_017025786.1:c.1758-227del	XP_016881275.1:n.1758-227del
XM_017025787.1:c.1758-227del	XP_016881276.1:n.1758-227del
NM_000271.5:c.1758-227del MANE Select	NP_000262.2:n.1758-227del