Canonical Allele Identifier: CA2290165961

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23539944G= , CM000680.2:g.23539944G=	GRCh38
NC_000018.9:g.21119908G= , CM000680.1:g.21119908G=	GRCh37
NC_000018.8:g.19373906G=	NCBI36
NG_012795.1:g.51674C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.2662C= MANE Select	ENSP00000269228.4:p.Pro888=
ENST00000269228.9:c.2662C=	ENSP00000269228.4:p.Pro888=
ENST00000540608.5:n.2576C=
ENST00000586718.1:n.453C=
ENST00000591051.1:c.1740C=
NM_000271.4:c.2662C=	NP_000262.2:p.Pro888=
XM_005258277.1:c.2713C=	XP_005258334.1:p.Pro905=
XM_005258278.3:c.2713C=	XP_005258335.1:p.Pro905=
XM_005258279.1:c.2662C=	XP_005258336.1:p.Pro888=
XM_006722479.2:c.2713C=	XP_006722542.1:p.Pro905=
XM_011526015.1:c.2248C=	XP_011524317.1:p.Pro750=
XM_005258278.5:c.2713C=	XP_005258335.1:p.Pro905=
XM_005258279.2:c.2662C=	XP_005258336.1:p.Pro888=
XM_006722479.3:c.2713C=	XP_006722542.1:p.Pro905=
XM_017025784.1:c.2713C=	XP_016881273.1:p.Pro905=
XM_017025785.1:c.2713C=	XP_016881274.1:p.Pro905=
XM_017025786.1:c.2662C=	XP_016881275.1:p.Pro888=
XM_017025787.1:c.2662C=	XP_016881276.1:p.Pro888=
NM_000271.5:c.2662C= MANE Select	NP_000262.2:p.Pro888=