Canonical Allele Identifier: CA2290176130

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23561321A= , CM000680.2:g.23561321A=	GRCh38
NC_000018.9:g.21141285A= , CM000680.1:g.21141285A=	GRCh37
NC_000018.8:g.19395283A=	NCBI36
NG_012795.1:g.30297T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.631+39T= MANE Select	ENSP00000269228.4:n.631+39T=
ENST00000269228.9:c.631+39T=	ENSP00000269228.4:n.631+39T=
ENST00000540608.5:n.545+39T=
NM_000271.4:c.631+39T=	NP_000262.2:n.631+39T=
XM_005258277.1:c.631+39T=	XP_005258334.1:n.631+39T=
XM_005258278.3:c.631+39T=	XP_005258335.1:n.631+39T=
XM_005258279.1:c.631+39T=	XP_005258336.1:n.631+39T=
XM_006722479.2:c.631+39T=	XP_006722542.1:n.631+39T=
XM_011526015.1:c.166+39T=	XP_011524317.1:n.166+39T=
XM_005258278.5:c.631+39T=	XP_005258335.1:n.631+39T=
XM_005258279.2:c.631+39T=	XP_005258336.1:n.631+39T=
XM_006722479.3:c.631+39T=	XP_006722542.1:n.631+39T=
XM_017025784.1:c.631+39T=	XP_016881273.1:n.631+39T=
XM_017025785.1:c.631+39T=	XP_016881274.1:n.631+39T=
XM_017025786.1:c.631+39T=	XP_016881275.1:n.631+39T=
XM_017025787.1:c.631+39T=	XP_016881276.1:n.631+39T=
NM_000271.5:c.631+39T= MANE Select	NP_000262.2:n.631+39T=