Canonical Allele Identifier: CA8913512

Gene: NPC1

Linked Data

• ClinVar Variation Id: 235359
• ClinVar RCV Id: RCV000224097 ; RCV000390564 ; RCV001086756
• dbSNP Id: rs77080672
• ExAC: 18:21136301 C / T
• gnomAD v2: 18-21136301-C-T
• gnomAD v3: 18-23556337-C-T
• gnomAD v4: 18-23556337-C-T
• MyVariant Identifiers: chr18:g.21136301C>T (hg19) ; chr18:g.21136301_21136302delinsTG (hg19) ; chr18:g.23556337C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23556337C>T , CM000680.2:g.23556337C>T	GRCh38
NC_000018.9:g.21136301C>T , CM000680.1:g.21136301C>T	GRCh37
NC_000018.8:g.19390299C>T	NCBI36
NG_012795.1:g.35281G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.1232G>A MANE Select	ENSP00000269228.4:p.Arg411Gln
ENST00000269228.9:c.1232G>A	ENSP00000269228.4:p.Arg411Gln
ENST00000540608.5:n.1146G>A
ENST00000591051.1:c.514G>A
NM_000271.4:c.1232G>A	NP_000262.2:p.Arg411Gln
XM_005258277.1:c.1283G>A	XP_005258334.1:p.Arg428Gln
XM_005258278.3:c.1283G>A	XP_005258335.1:p.Arg428Gln
XM_005258279.1:c.1232G>A	XP_005258336.1:p.Arg411Gln
XM_006722479.2:c.1283G>A	XP_006722542.1:p.Arg428Gln
XM_011526015.1:c.818G>A	XP_011524317.1:p.Arg273Gln
XM_005258278.5:c.1283G>A	XP_005258335.1:p.Arg428Gln
XM_005258279.2:c.1232G>A	XP_005258336.1:p.Arg411Gln
XM_006722479.3:c.1283G>A	XP_006722542.1:p.Arg428Gln
XM_017025784.1:c.1283G>A	XP_016881273.1:p.Arg428Gln
XM_017025785.1:c.1283G>A	XP_016881274.1:p.Arg428Gln
XM_017025786.1:c.1232G>A	XP_016881275.1:p.Arg411Gln
XM_017025787.1:c.1232G>A	XP_016881276.1:p.Arg411Gln
NM_000271.5:c.1232G>A MANE Select	NP_000262.2:p.Arg411Gln