Canonical Allele Identifier: CA2290168485

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23545254_23545256delinsTGG , CM000680.2:g.23545254_23545256delinsTGG	GRCh38
NC_000018.9:g.21125218_21125220delinsTGG , CM000680.1:g.21125218_21125220delinsTGG	GRCh37
NC_000018.8:g.19379216_19379218delinsTGG	NCBI36
NG_012795.1:g.46362_46364delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.1758-107_1758-105delinsCCA MANE Select	ENSP00000269228.4:n.1758-107_1758-105delinsCCA
ENST00000269228.9:c.1758-107_1758-105delinsCCA	ENSP00000269228.4:n.1758-107_1758-105delinsCCA
ENST00000540608.5:n.1672-107_1672-105delinsCCA
ENST00000591051.1:c.836-107_836-105delinsCCA
NM_000271.4:c.1758-107_1758-105delinsCCA	NP_000262.2:n.1758-107_1758-105delinsCCA
XM_005258277.1:c.1809-107_1809-105delinsCCA	XP_005258334.1:n.1809-107_1809-105delinsCCA
XM_005258278.3:c.1809-107_1809-105delinsCCA	XP_005258335.1:n.1809-107_1809-105delinsCCA
XM_005258279.1:c.1758-107_1758-105delinsCCA	XP_005258336.1:n.1758-107_1758-105delinsCCA
XM_006722479.2:c.1809-107_1809-105delinsCCA	XP_006722542.1:n.1809-107_1809-105delinsCCA
XM_011526015.1:c.1344-107_1344-105delinsCCA	XP_011524317.1:n.1344-107_1344-105delinsCCA
XM_005258278.5:c.1809-107_1809-105delinsCCA	XP_005258335.1:n.1809-107_1809-105delinsCCA
XM_005258279.2:c.1758-107_1758-105delinsCCA	XP_005258336.1:n.1758-107_1758-105delinsCCA
XM_006722479.3:c.1809-107_1809-105delinsCCA	XP_006722542.1:n.1809-107_1809-105delinsCCA
XM_017025784.1:c.1809-107_1809-105delinsCCA	XP_016881273.1:n.1809-107_1809-105delinsCCA
XM_017025785.1:c.1809-107_1809-105delinsCCA	XP_016881274.1:n.1809-107_1809-105delinsCCA
XM_017025786.1:c.1758-107_1758-105delinsCCA	XP_016881275.1:n.1758-107_1758-105delinsCCA
XM_017025787.1:c.1758-107_1758-105delinsCCA	XP_016881276.1:n.1758-107_1758-105delinsCCA
NM_000271.5:c.1758-107_1758-105delinsCCA MANE Select	NP_000262.2:n.1758-107_1758-105delinsCCA