Canonical Allele Identifier: CA2290162813

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23533473C= , CM000680.2:g.23533473C=	GRCh38
NC_000018.9:g.21113437C= , CM000680.1:g.21113437C=	GRCh37
NC_000018.8:g.19367435C=	NCBI36
NG_012795.1:g.58145G=
NG_033119.1:g.35004C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.3636G= MANE Select	ENSP00000269228.4:p.Val1212=
ENST00000269228.9:c.3636G=	ENSP00000269228.4:p.Val1212=
ENST00000586150.5:c.391G=
ENST00000587163.1:n.160G=
ENST00000588867.1:n.1319G=
ENST00000590723.5:c.45G=	ENSP00000464755.1:p.Val15=
ENST00000591051.1:c.2714G=
ENST00000591107.6:c.313G=
NM_000271.4:c.3636G=	NP_000262.2:p.Val1212=
XM_005258277.1:c.3687G=	XP_005258334.1:p.Val1229=
XM_005258278.3:c.3687G=	XP_005258335.1:p.Val1229=
XM_005258279.1:c.3636G=	XP_005258336.1:p.Val1212=
XM_006722479.2:c.3687G=	XP_006722542.1:p.Val1229=
XM_011526015.1:c.3222G=	XP_011524317.1:p.Val1074=
XM_005258278.5:c.3687G=	XP_005258335.1:p.Val1229=
XM_005258279.2:c.3636G=	XP_005258336.1:p.Val1212=
XM_006722479.3:c.3687G=	XP_006722542.1:p.Val1229=
XM_017025784.1:c.3687G=	XP_016881273.1:p.Val1229=
XM_017025785.1:c.3687G=	XP_016881274.1:p.Val1229=
XM_017025786.1:c.3636G=	XP_016881275.1:p.Val1212=
XM_017025787.1:c.3636G=	XP_016881276.1:p.Val1212=
NM_000271.5:c.3636G= MANE Select	NP_000262.2:p.Val1212=