Canonical Allele Identifier: CA2290180351

Gene: NPC1

Linked Data

• dbSNP Id: rs2059160351
• gnomAD v3: 18-23568688-G-GC
• gnomAD v4: 18-23568688-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23568689dup , CM000680.2:g.23568689dup	GRCh38
NC_000018.9:g.21148653dup , CM000680.1:g.21148653dup	GRCh37
NC_000018.8:g.19402651dup	NCBI36
NG_012795.1:g.22929dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.463+134dup MANE Select	ENSP00000269228.4:n.463+134dup
ENST00000269228.9:c.463+134dup	ENSP00000269228.4:n.463+134dup
ENST00000540608.5:n.377+134dup
NM_000271.4:c.463+134dup	NP_000262.2:n.463+134dup
XM_005258277.1:c.463+134dup	XP_005258334.1:n.463+134dup
XM_005258278.3:c.463+134dup	XP_005258335.1:n.463+134dup
XM_005258279.1:c.463+134dup	XP_005258336.1:n.463+134dup
XM_006722479.2:c.463+134dup	XP_006722542.1:n.463+134dup
XM_011526015.1:c.-3+134dup	XP_011524317.1:n.-3+134dup
XM_005258278.5:c.463+134dup	XP_005258335.1:n.463+134dup
XM_005258279.2:c.463+134dup	XP_005258336.1:n.463+134dup
XM_006722479.3:c.463+134dup	XP_006722542.1:n.463+134dup
XM_017025784.1:c.463+134dup	XP_016881273.1:n.463+134dup
XM_017025785.1:c.463+134dup	XP_016881274.1:n.463+134dup
XM_017025786.1:c.463+134dup	XP_016881275.1:n.463+134dup
XM_017025787.1:c.463+134dup	XP_016881276.1:n.463+134dup
NM_000271.5:c.463+134dup MANE Select	NP_000262.2:n.463+134dup