Canonical Allele Identifier: CA2695227429

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23536792del , CM000680.2:g.23536792del	GRCh38
NC_000018.9:g.21116756del , CM000680.1:g.21116756del	GRCh37
NC_000018.8:g.19370754del	NCBI36
NG_012795.1:g.54826del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.3126del MANE Select	ENSP00000269228.4:p.His1042GlnfsTer14
ENST00000269228.9:c.3126del	ENSP00000269228.4:p.His1042GlnfsTer14
ENST00000591051.1:c.2204del
ENST00000591075.1:n.759del
ENST00000591955.1:n.469del
NM_000271.4:c.3126del	NP_000262.2:p.His1042GlnfsTer14
XM_005258277.1:c.3177del	XP_005258334.1:p.His1059GlnfsTer14
XM_005258278.3:c.3177del	XP_005258335.1:p.His1059GlnfsTer14
XM_005258279.1:c.3126del	XP_005258336.1:p.His1042GlnfsTer14
XM_006722479.2:c.3177del	XP_006722542.1:p.His1059GlnfsTer14
XM_011526015.1:c.2712del	XP_011524317.1:p.His904GlnfsTer14
XM_005258278.5:c.3177del	XP_005258335.1:p.His1059GlnfsTer14
XM_005258279.2:c.3126del	XP_005258336.1:p.His1042GlnfsTer14
XM_006722479.3:c.3177del	XP_006722542.1:p.His1059GlnfsTer14
XM_017025784.1:c.3177del	XP_016881273.1:p.His1059GlnfsTer14
XM_017025785.1:c.3177del	XP_016881274.1:p.His1059GlnfsTer14
XM_017025786.1:c.3126del	XP_016881275.1:p.His1042GlnfsTer14
XM_017025787.1:c.3126del	XP_016881276.1:p.His1042GlnfsTer14
NM_000271.5:c.3126del MANE Select	NP_000262.2:p.His1042GlnfsTer14