Canonical Allele Identifier: CA2290165307
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23538489A= , CM000680.2:g.23538489A= GRCh38
NC_000018.9:g.21118453A= , CM000680.1:g.21118453A= GRCh37
NC_000018.8:g.19372451A= NCBI36
NG_012795.1:g.53129T=

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.3041+53T= MANE Select ENSP00000269228.4:n.3041+53T=
ENST00000269228.9:c.3041+53T= ENSP00000269228.4:n.3041+53T=
ENST00000591051.1:c.2119+53T=
ENST00000591075.1:n.674+53T=
ENST00000591955.1:n.384+53T=
NM_000271.4:c.3041+53T= NP_000262.2:n.3041+53T=
XM_005258277.1:c.3092+53T= XP_005258334.1:n.3092+53T=
XM_005258278.3:c.3092+53T= XP_005258335.1:n.3092+53T=
XM_005258279.1:c.3041+53T= XP_005258336.1:n.3041+53T=
XM_006722479.2:c.3092+53T= XP_006722542.1:n.3092+53T=
XM_011526015.1:c.2627+53T= XP_011524317.1:n.2627+53T=
XM_005258278.5:c.3092+53T= XP_005258335.1:n.3092+53T=
XM_005258279.2:c.3041+53T= XP_005258336.1:n.3041+53T=
XM_006722479.3:c.3092+53T= XP_006722542.1:n.3092+53T=
XM_017025784.1:c.3092+53T= XP_016881273.1:n.3092+53T=
XM_017025785.1:c.3092+53T= XP_016881274.1:n.3092+53T=
XM_017025786.1:c.3041+53T= XP_016881275.1:n.3041+53T=
XM_017025787.1:c.3041+53T= XP_016881276.1:n.3041+53T=
NM_000271.5:c.3041+53T= MANE Select NP_000262.2:n.3041+53T=