Canonical Allele Identifier: CA2840378436

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23539791del , CM000680.2:g.23539791del	GRCh38
NC_000018.9:g.21119755del , CM000680.1:g.21119755del	GRCh37
NC_000018.8:g.19373753del	NCBI36
NG_012795.1:g.51827del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.2795+20del MANE Select	ENSP00000269228.4:n.2795+20del
ENST00000269228.9:c.2795+20del	ENSP00000269228.4:n.2795+20del
ENST00000540608.5:n.2729del
ENST00000591051.1:c.1873+20del
ENST00000591075.1:n.108del
NM_000271.4:c.2795+20del	NP_000262.2:n.2795+20del
XM_005258277.1:c.2846+20del	XP_005258334.1:n.2846+20del
XM_005258278.3:c.2846+20del	XP_005258335.1:n.2846+20del
XM_005258279.1:c.2795+20del	XP_005258336.1:n.2795+20del
XM_006722479.2:c.2846+20del	XP_006722542.1:n.2846+20del
XM_011526015.1:c.2381+20del	XP_011524317.1:n.2381+20del
XM_005258278.5:c.2846+20del	XP_005258335.1:n.2846+20del
XM_005258279.2:c.2795+20del	XP_005258336.1:n.2795+20del
XM_006722479.3:c.2846+20del	XP_006722542.1:n.2846+20del
XM_017025784.1:c.2846+20del	XP_016881273.1:n.2846+20del
XM_017025785.1:c.2846+20del	XP_016881274.1:n.2846+20del
XM_017025786.1:c.2795+20del	XP_016881275.1:n.2795+20del
XM_017025787.1:c.2795+20del	XP_016881276.1:n.2795+20del
NM_000271.5:c.2795+20del MANE Select	NP_000262.2:n.2795+20del