Canonical Allele Identifier: CA401792659

Gene: NPC1

Linked Data

• ClinVar Variation Id: 2751556
• ClinVar RCV Id: RCV003500036
• gnomAD v4: 18-23539827-C-T
• MyVariant Identifiers: chr18:g.21119791C>T (hg19) ; chr18:g.23539827C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23539827C>T , CM000680.2:g.23539827C>T	GRCh38
NC_000018.9:g.21119791C>T , CM000680.1:g.21119791C>T	GRCh37
NC_000018.8:g.19373789C>T	NCBI36
NG_012795.1:g.51791G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.2779G>A MANE Select	ENSP00000269228.4:p.Ala927Thr
ENST00000269228.9:c.2779G>A	ENSP00000269228.4:p.Ala927Thr
ENST00000540608.5:n.2693G>A
ENST00000586718.1:n.570G>A
ENST00000591051.1:c.1857G>A
ENST00000591075.1:n.72G>A
NM_000271.4:c.2779G>A	NP_000262.2:p.Ala927Thr
XM_005258277.1:c.2830G>A	XP_005258334.1:p.Ala944Thr
XM_005258278.3:c.2830G>A	XP_005258335.1:p.Ala944Thr
XM_005258279.1:c.2779G>A	XP_005258336.1:p.Ala927Thr
XM_006722479.2:c.2830G>A	XP_006722542.1:p.Ala944Thr
XM_011526015.1:c.2365G>A	XP_011524317.1:p.Ala789Thr
XM_005258278.5:c.2830G>A	XP_005258335.1:p.Ala944Thr
XM_005258279.2:c.2779G>A	XP_005258336.1:p.Ala927Thr
XM_006722479.3:c.2830G>A	XP_006722542.1:p.Ala944Thr
XM_017025784.1:c.2830G>A	XP_016881273.1:p.Ala944Thr
XM_017025785.1:c.2830G>A	XP_016881274.1:p.Ala944Thr
XM_017025786.1:c.2779G>A	XP_016881275.1:p.Ala927Thr
XM_017025787.1:c.2779G>A	XP_016881276.1:p.Ala927Thr
NM_000271.5:c.2779G>A MANE Select	NP_000262.2:p.Ala927Thr