Canonical Allele Identifier: CA2697555389
Gene: NPC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2748642
ClinVar RCV Id: RCV003501986

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23545149_23545155del , CM000680.2:g.23545149_23545155del GRCh38
NC_000018.9:g.21125113_21125119del , CM000680.1:g.21125113_21125119del GRCh37
NC_000018.8:g.19379111_19379117del NCBI36
NG_012795.1:g.46466_46472del

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.1758-3_1761del
ENST00000269228.9:c.1758-3_1761del
ENST00000540608.5:n.1672-3_1675del
ENST00000591051.1:c.836-3_839del
NM_000271.4:c.1758-3_1761del
XM_005258277.1:c.1809-3_1812del
XM_005258278.3:c.1809-3_1812del
XM_005258279.1:c.1758-3_1761del
XM_006722479.2:c.1809-3_1812del
XM_011526015.1:c.1344-3_1347del
XM_005258278.5:c.1809-3_1812del
XM_005258279.2:c.1758-3_1761del
XM_006722479.3:c.1809-3_1812del
XM_017025784.1:c.1809-3_1812del
XM_017025785.1:c.1809-3_1812del
XM_017025786.1:c.1758-3_1761del
XM_017025787.1:c.1758-3_1761del
NM_000271.5:c.1758-3_1761del