Canonical Allele Identifier: CA297080763

Gene: NPC1

Linked Data

• ClinVar Variation Id: 2109363
• ClinVar RCV Id: RCV003038320
• dbSNP Id: rs367911777
• MyVariant Identifiers: chr18:g.21118634C>T (hg19) ; chr18:g.23538670C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23538670C>T , CM000680.2:g.23538670C>T	GRCh38
NC_000018.9:g.21118634C>T , CM000680.1:g.21118634C>T	GRCh37
NC_000018.8:g.19372632C>T	NCBI36
NG_012795.1:g.52948G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.2913G>A MANE Select	ENSP00000269228.4:p.Val971=
ENST00000269228.9:c.2913G>A	ENSP00000269228.4:p.Val971=
ENST00000591051.1:c.1991G>A
ENST00000591075.1:n.546G>A
ENST00000591955.1:n.256G>A
NM_000271.4:c.2913G>A	NP_000262.2:p.Val971=
XM_005258277.1:c.2964G>A	XP_005258334.1:p.Val988=
XM_005258278.3:c.2964G>A	XP_005258335.1:p.Val988=
XM_005258279.1:c.2913G>A	XP_005258336.1:p.Val971=
XM_006722479.2:c.2964G>A	XP_006722542.1:p.Val988=
XM_011526015.1:c.2499G>A	XP_011524317.1:p.Val833=
XM_005258278.5:c.2964G>A	XP_005258335.1:p.Val988=
XM_005258279.2:c.2913G>A	XP_005258336.1:p.Val971=
XM_006722479.3:c.2964G>A	XP_006722542.1:p.Val988=
XM_017025784.1:c.2964G>A	XP_016881273.1:p.Val988=
XM_017025785.1:c.2964G>A	XP_016881274.1:p.Val988=
XM_017025786.1:c.2913G>A	XP_016881275.1:p.Val971=
XM_017025787.1:c.2913G>A	XP_016881276.1:p.Val971=
NM_000271.5:c.2913G>A MANE Select	NP_000262.2:p.Val971=