Canonical Allele Identifier: CA628677899

Gene: NPC1

Linked Data

• dbSNP Id: rs1567949635
• gnomAD v2: 18-21119471-AG-A
• MyVariant Identifiers: chr18:g.21119472del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23539510del , CM000680.2:g.23539510del	GRCh38
NC_000018.9:g.21119474del , CM000680.1:g.21119474del	GRCh37
NC_000018.8:g.19373472del	NCBI36
NG_012795.1:g.52110del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.2796-38del MANE Select	ENSP00000269228.4:n.2796-38del
ENST00000269228.9:c.2796-38del	ENSP00000269228.4:n.2796-38del
ENST00000591051.1:c.1874-38del
ENST00000591075.1:n.391del
NM_000271.4:c.2796-38del	NP_000262.2:n.2796-38del
XM_005258277.1:c.2847-38del	XP_005258334.1:n.2847-38del
XM_005258278.3:c.2847-38del	XP_005258335.1:n.2847-38del
XM_005258279.1:c.2796-38del	XP_005258336.1:n.2796-38del
XM_006722479.2:c.2847-38del	XP_006722542.1:n.2847-38del
XM_011526015.1:c.2382-38del	XP_011524317.1:n.2382-38del
XM_005258278.5:c.2847-38del	XP_005258335.1:n.2847-38del
XM_005258279.2:c.2796-38del	XP_005258336.1:n.2796-38del
XM_006722479.3:c.2847-38del	XP_006722542.1:n.2847-38del
XM_017025784.1:c.2847-38del	XP_016881273.1:n.2847-38del
XM_017025785.1:c.2847-38del	XP_016881274.1:n.2847-38del
XM_017025786.1:c.2796-38del	XP_016881275.1:n.2796-38del
XM_017025787.1:c.2796-38del	XP_016881276.1:n.2796-38del
NM_000271.5:c.2796-38del MANE Select	NP_000262.2:n.2796-38del