Canonical Allele Identifier: CA2290173687

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23556340A= , CM000680.2:g.23556340A=	GRCh38
NC_000018.9:g.21136304A= , CM000680.1:g.21136304A=	GRCh37
NC_000018.8:g.19390302A=	NCBI36
NG_012795.1:g.35278T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.1229T= MANE Select	ENSP00000269228.4:p.Ile410=
ENST00000269228.9:c.1229T=	ENSP00000269228.4:p.Ile410=
ENST00000540608.5:n.1143T=
ENST00000591051.1:c.511T=
NM_000271.4:c.1229T=	NP_000262.2:p.Ile410=
XM_005258277.1:c.1280T=	XP_005258334.1:p.Ile427=
XM_005258278.3:c.1280T=	XP_005258335.1:p.Ile427=
XM_005258279.1:c.1229T=	XP_005258336.1:p.Ile410=
XM_006722479.2:c.1280T=	XP_006722542.1:p.Ile427=
XM_011526015.1:c.815T=	XP_011524317.1:p.Ile272=
XM_005258278.5:c.1280T=	XP_005258335.1:p.Ile427=
XM_005258279.2:c.1229T=	XP_005258336.1:p.Ile410=
XM_006722479.3:c.1280T=	XP_006722542.1:p.Ile427=
XM_017025784.1:c.1280T=	XP_016881273.1:p.Ile427=
XM_017025785.1:c.1280T=	XP_016881274.1:p.Ile427=
XM_017025786.1:c.1229T=	XP_016881275.1:p.Ile410=
XM_017025787.1:c.1229T=	XP_016881276.1:p.Ile410=
NM_000271.5:c.1229T= MANE Select	NP_000262.2:p.Ile410=