Canonical Allele Identifier: CA2290163858

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23535502A= , CM000680.2:g.23535502A=	GRCh38
NC_000018.9:g.21115466A= , CM000680.1:g.21115466A=	GRCh37
NC_000018.8:g.19369464A=	NCBI36
NG_012795.1:g.56116T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.3444T= MANE Select	ENSP00000269228.4:p.Ser1148=
ENST00000269228.9:c.3444T=	ENSP00000269228.4:p.Ser1148=
ENST00000586150.5:c.199T=
ENST00000588867.1:n.199T=
ENST00000591051.1:c.2522T=
ENST00000591107.6:c.121T=
NM_000271.4:c.3444T=	NP_000262.2:p.Ser1148=
XM_005258277.1:c.3495T=	XP_005258334.1:p.Ser1165=
XM_005258278.3:c.3495T=	XP_005258335.1:p.Ser1165=
XM_005258279.1:c.3444T=	XP_005258336.1:p.Ser1148=
XM_006722479.2:c.3495T=	XP_006722542.1:p.Ser1165=
XM_011526015.1:c.3030T=	XP_011524317.1:p.Ser1010=
XM_005258278.5:c.3495T=	XP_005258335.1:p.Ser1165=
XM_005258279.2:c.3444T=	XP_005258336.1:p.Ser1148=
XM_006722479.3:c.3495T=	XP_006722542.1:p.Ser1165=
XM_017025784.1:c.3495T=	XP_016881273.1:p.Ser1165=
XM_017025785.1:c.3495T=	XP_016881274.1:p.Ser1165=
XM_017025786.1:c.3444T=	XP_016881275.1:p.Ser1148=
XM_017025787.1:c.3444T=	XP_016881276.1:p.Ser1148=
NM_000271.5:c.3444T= MANE Select	NP_000262.2:p.Ser1148=