Canonical Allele Identifier: CA2290165306
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23538486T= , CM000680.2:g.23538486T= GRCh38
NC_000018.9:g.21118450T= , CM000680.1:g.21118450T= GRCh37
NC_000018.8:g.19372448T= NCBI36
NG_012795.1:g.53132A=

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.3041+56A= MANE Select ENSP00000269228.4:n.3041+56A=
ENST00000269228.9:c.3041+56A= ENSP00000269228.4:n.3041+56A=
ENST00000591051.1:c.2119+56A=
ENST00000591075.1:n.674+56A=
ENST00000591955.1:n.384+56A=
NM_000271.4:c.3041+56A= NP_000262.2:n.3041+56A=
XM_005258277.1:c.3092+56A= XP_005258334.1:n.3092+56A=
XM_005258278.3:c.3092+56A= XP_005258335.1:n.3092+56A=
XM_005258279.1:c.3041+56A= XP_005258336.1:n.3041+56A=
XM_006722479.2:c.3092+56A= XP_006722542.1:n.3092+56A=
XM_011526015.1:c.2627+56A= XP_011524317.1:n.2627+56A=
XM_005258278.5:c.3092+56A= XP_005258335.1:n.3092+56A=
XM_005258279.2:c.3041+56A= XP_005258336.1:n.3041+56A=
XM_006722479.3:c.3092+56A= XP_006722542.1:n.3092+56A=
XM_017025784.1:c.3092+56A= XP_016881273.1:n.3092+56A=
XM_017025785.1:c.3092+56A= XP_016881274.1:n.3092+56A=
XM_017025786.1:c.3041+56A= XP_016881275.1:n.3041+56A=
XM_017025787.1:c.3041+56A= XP_016881276.1:n.3041+56A=
NM_000271.5:c.3041+56A= MANE Select NP_000262.2:n.3041+56A=