Canonical Allele Identifier: CA2290162815

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23533479A= , CM000680.2:g.23533479A=	GRCh38
NC_000018.9:g.21113443A= , CM000680.1:g.21113443A=	GRCh37
NC_000018.8:g.19367441A=	NCBI36
NG_012795.1:g.58139T=
NG_033119.1:g.35010A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.3630T= MANE Select	ENSP00000269228.4:p.Ile1210=
ENST00000269228.9:c.3630T=	ENSP00000269228.4:p.Ile1210=
ENST00000586150.5:c.385T=
ENST00000587163.1:n.154T=
ENST00000588867.1:n.1313T=
ENST00000590723.5:c.39T=	ENSP00000464755.1:p.Ile13=
ENST00000591051.1:c.2708T=
ENST00000591107.6:c.307T=
NM_000271.4:c.3630T=	NP_000262.2:p.Ile1210=
XM_005258277.1:c.3681T=	XP_005258334.1:p.Ile1227=
XM_005258278.3:c.3681T=	XP_005258335.1:p.Ile1227=
XM_005258279.1:c.3630T=	XP_005258336.1:p.Ile1210=
XM_006722479.2:c.3681T=	XP_006722542.1:p.Ile1227=
XM_011526015.1:c.3216T=	XP_011524317.1:p.Ile1072=
XM_005258278.5:c.3681T=	XP_005258335.1:p.Ile1227=
XM_005258279.2:c.3630T=	XP_005258336.1:p.Ile1210=
XM_006722479.3:c.3681T=	XP_006722542.1:p.Ile1227=
XM_017025784.1:c.3681T=	XP_016881273.1:p.Ile1227=
XM_017025785.1:c.3681T=	XP_016881274.1:p.Ile1227=
XM_017025786.1:c.3630T=	XP_016881275.1:p.Ile1210=
XM_017025787.1:c.3630T=	XP_016881276.1:p.Ile1210=
NM_000271.5:c.3630T= MANE Select	NP_000262.2:p.Ile1210=