Canonical Allele Identifier: CA2290175773

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23560487A= , CM000680.2:g.23560487A=	GRCh38
NC_000018.9:g.21140451A= , CM000680.1:g.21140451A=	GRCh37
NC_000018.8:g.19394449A=	NCBI36
NG_012795.1:g.31131T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.632-7T= MANE Select	ENSP00000269228.4:n.632-7T=
ENST00000269228.9:c.632-7T=	ENSP00000269228.4:n.632-7T=
ENST00000540608.5:n.546-7T=
NM_000271.4:c.632-7T=	NP_000262.2:n.632-7T=
XM_005258277.1:c.632-7T=	XP_005258334.1:n.632-7T=
XM_005258278.3:c.632-7T=	XP_005258335.1:n.632-7T=
XM_005258279.1:c.632-7T=	XP_005258336.1:n.632-7T=
XM_006722479.2:c.632-7T=	XP_006722542.1:n.632-7T=
XM_011526015.1:c.167-7T=	XP_011524317.1:n.167-7T=
XM_005258278.5:c.632-7T=	XP_005258335.1:n.632-7T=
XM_005258279.2:c.632-7T=	XP_005258336.1:n.632-7T=
XM_006722479.3:c.632-7T=	XP_006722542.1:n.632-7T=
XM_017025784.1:c.632-7T=	XP_016881273.1:n.632-7T=
XM_017025785.1:c.632-7T=	XP_016881274.1:n.632-7T=
XM_017025786.1:c.632-7T=	XP_016881275.1:n.632-7T=
XM_017025787.1:c.632-7T=	XP_016881276.1:n.632-7T=
NM_000271.5:c.632-7T= MANE Select	NP_000262.2:n.632-7T=