Canonical Allele Identifier: CA2290168558
Gene: NPC1 HGNC NCBI

Linked Data

dbSNP Id: rs2058775286

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23545401C>A , CM000680.2:g.23545401C>A GRCh38
NC_000018.9:g.21125365C>A , CM000680.1:g.21125365C>A GRCh37
NC_000018.8:g.19379363C>A NCBI36
NG_012795.1:g.46217G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.1758-252G>T MANE Select ENSP00000269228.4:n.1758-252G>T
ENST00000269228.9:c.1758-252G>T ENSP00000269228.4:n.1758-252G>T
ENST00000540608.5:n.1672-252G>T
ENST00000591051.1:c.836-252G>T
NM_000271.4:c.1758-252G>T NP_000262.2:n.1758-252G>T
XM_005258277.1:c.1809-252G>T XP_005258334.1:n.1809-252G>T
XM_005258278.3:c.1809-252G>T XP_005258335.1:n.1809-252G>T
XM_005258279.1:c.1758-252G>T XP_005258336.1:n.1758-252G>T
XM_006722479.2:c.1809-252G>T XP_006722542.1:n.1809-252G>T
XM_011526015.1:c.1344-252G>T XP_011524317.1:n.1344-252G>T
XM_005258278.5:c.1809-252G>T XP_005258335.1:n.1809-252G>T
XM_005258279.2:c.1758-252G>T XP_005258336.1:n.1758-252G>T
XM_006722479.3:c.1809-252G>T XP_006722542.1:n.1809-252G>T
XM_017025784.1:c.1809-252G>T XP_016881273.1:n.1809-252G>T
XM_017025785.1:c.1809-252G>T XP_016881274.1:n.1809-252G>T
XM_017025786.1:c.1758-252G>T XP_016881275.1:n.1758-252G>T
XM_017025787.1:c.1758-252G>T XP_016881276.1:n.1758-252G>T
NM_000271.5:c.1758-252G>T MANE Select NP_000262.2:n.1758-252G>T