Canonical Allele Identifier: CA401790512

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23533364T>C , CM000680.2:g.23533364T>C	GRCh38
NC_000018.9:g.21113328T>C , CM000680.1:g.21113328T>C	GRCh37
NC_000018.8:g.19367326T>C	NCBI36
NG_012795.1:g.58254A>G
NG_033119.1:g.34895T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000271.5:c.3745A>G MANE Select	NP_000262.2:p.Ser1249Gly
ENST00000269228.10:c.3745A>G MANE Select	ENSP00000269228.4:p.Ser1249Gly
NM_000271.4:c.3745A>G	NP_000262.2:p.Ser1249Gly
ENST00000269228.9:c.3745A>G	ENSP00000269228.4:p.Ser1249Gly
ENST00000586150.5:c.500A>G
ENST00000587163.1:n.269A>G
ENST00000588867.1:n.1428A>G
ENST00000590723.5:c.154A>G	ENSP00000464755.1:p.Ser52Gly
ENST00000591051.1:c.2823A>G
ENST00000591107.6:c.422A>G
ENST00000593280.2:c.77A>G
XM_005258277.1:c.3796A>G	XP_005258334.1:p.Ser1266Gly
XM_005258278.3:c.3796A>G	XP_005258335.1:p.Ser1266Gly
XM_005258278.5:c.3796A>G	XP_005258335.1:p.Ser1266Gly
XM_005258279.1:c.3745A>G	XP_005258336.1:p.Ser1249Gly
XM_005258279.2:c.3745A>G	XP_005258336.1:p.Ser1249Gly
XM_006722479.2:c.3796A>G	XP_006722542.1:p.Ser1266Gly
XM_006722479.3:c.3796A>G	XP_006722542.1:p.Ser1266Gly
XM_011526015.1:c.3331A>G	XP_011524317.1:p.Ser1111Gly
XM_017025784.1:c.3796A>G	XP_016881273.1:p.Ser1266Gly
XM_017025785.1:c.3796A>G	XP_016881274.1:p.Ser1266Gly
XM_017025786.1:c.3745A>G	XP_016881275.1:p.Ser1249Gly
XM_017025787.1:c.3745A>G	XP_016881276.1:p.Ser1249Gly