Canonical Allele Identifier: CA2290173124
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23554897G= , CM000680.2:g.23554897G= GRCh38
NC_000018.9:g.21134861G= , CM000680.1:g.21134861G= GRCh37
NC_000018.8:g.19388859G= NCBI36
NG_012795.1:g.36721C=

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.1414C= MANE Select ENSP00000269228.4:p.Leu472=
ENST00000269228.9:c.1414C= ENSP00000269228.4:p.Leu472=
ENST00000540608.5:n.1328C=
ENST00000590301.1:n.89C=
ENST00000591051.1:c.696C=
NM_000271.4:c.1414C= NP_000262.2:p.Leu472=
XM_005258277.1:c.1465C= XP_005258334.1:p.Leu489=
XM_005258278.3:c.1465C= XP_005258335.1:p.Leu489=
XM_005258279.1:c.1414C= XP_005258336.1:p.Leu472=
XM_006722479.2:c.1465C= XP_006722542.1:p.Leu489=
XM_011526015.1:c.1000C= XP_011524317.1:p.Leu334=
XM_005258278.5:c.1465C= XP_005258335.1:p.Leu489=
XM_005258279.2:c.1414C= XP_005258336.1:p.Leu472=
XM_006722479.3:c.1465C= XP_006722542.1:p.Leu489=
XM_017025784.1:c.1465C= XP_016881273.1:p.Leu489=
XM_017025785.1:c.1465C= XP_016881274.1:p.Leu489=
XM_017025786.1:c.1414C= XP_016881275.1:p.Leu472=
XM_017025787.1:c.1414C= XP_016881276.1:p.Leu472=
NM_000271.5:c.1414C= MANE Select NP_000262.2:p.Leu472=