Canonical Allele Identifier: CA919946916

Gene: NPC1

Linked Data

• dbSNP Id: rs1567950601
• gnomAD v4: 18-23540149-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23540155del , CM000680.2:g.23540155del	GRCh38
NC_000018.9:g.21120119del , CM000680.1:g.21120119del	GRCh37
NC_000018.8:g.19374117del	NCBI36
NG_012795.1:g.51468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.2605-149del MANE Select	ENSP00000269228.4:n.2605-149del
ENST00000269228.9:c.2605-149del	ENSP00000269228.4:n.2605-149del
ENST00000540608.5:n.2519-149del
ENST00000586718.1:n.396-149del
ENST00000591051.1:c.1683-149del
NM_000271.4:c.2605-149del	NP_000262.2:n.2605-149del
XM_005258277.1:c.2656-149del	XP_005258334.1:n.2656-149del
XM_005258278.3:c.2656-149del	XP_005258335.1:n.2656-149del
XM_005258279.1:c.2605-149del	XP_005258336.1:n.2605-149del
XM_006722479.2:c.2656-149del	XP_006722542.1:n.2656-149del
XM_011526015.1:c.2191-149del	XP_011524317.1:n.2191-149del
XM_005258278.5:c.2656-149del	XP_005258335.1:n.2656-149del
XM_005258279.2:c.2605-149del	XP_005258336.1:n.2605-149del
XM_006722479.3:c.2656-149del	XP_006722542.1:n.2656-149del
XM_017025784.1:c.2656-149del	XP_016881273.1:n.2656-149del
XM_017025785.1:c.2656-149del	XP_016881274.1:n.2656-149del
XM_017025786.1:c.2605-149del	XP_016881275.1:n.2605-149del
XM_017025787.1:c.2605-149del	XP_016881276.1:n.2605-149del
NM_000271.5:c.2605-149del MANE Select	NP_000262.2:n.2605-149del