Canonical Allele Identifier: CA628978908

Gene: NPC1

Linked Data

• dbSNP Id: rs1264940163
• gnomAD v2: 18-21141277-T-A
• gnomAD v4: 18-23561313-T-A
• MyVariant Identifiers: chr18:g.21141277T>A (hg19) ; chr18:g.23561313T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23561313T>A , CM000680.2:g.23561313T>A	GRCh38
NC_000018.9:g.21141277T>A , CM000680.1:g.21141277T>A	GRCh37
NC_000018.8:g.19395275T>A	NCBI36
NG_012795.1:g.30305A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.631+47A>T MANE Select	ENSP00000269228.4:n.631+47A>T
ENST00000269228.9:c.631+47A>T	ENSP00000269228.4:n.631+47A>T
ENST00000540608.5:n.545+47A>T
NM_000271.4:c.631+47A>T	NP_000262.2:n.631+47A>T
XM_005258277.1:c.631+47A>T	XP_005258334.1:n.631+47A>T
XM_005258278.3:c.631+47A>T	XP_005258335.1:n.631+47A>T
XM_005258279.1:c.631+47A>T	XP_005258336.1:n.631+47A>T
XM_006722479.2:c.631+47A>T	XP_006722542.1:n.631+47A>T
XM_011526015.1:c.166+47A>T	XP_011524317.1:n.166+47A>T
XM_005258278.5:c.631+47A>T	XP_005258335.1:n.631+47A>T
XM_005258279.2:c.631+47A>T	XP_005258336.1:n.631+47A>T
XM_006722479.3:c.631+47A>T	XP_006722542.1:n.631+47A>T
XM_017025784.1:c.631+47A>T	XP_016881273.1:n.631+47A>T
XM_017025785.1:c.631+47A>T	XP_016881274.1:n.631+47A>T
XM_017025786.1:c.631+47A>T	XP_016881275.1:n.631+47A>T
XM_017025787.1:c.631+47A>T	XP_016881276.1:n.631+47A>T
NM_000271.5:c.631+47A>T MANE Select	NP_000262.2:n.631+47A>T