Canonical Allele Identifier: CA2290163742
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23535288G= , CM000680.2:g.23535288G= GRCh38
NC_000018.9:g.21115252G= , CM000680.1:g.21115252G= GRCh37
NC_000018.8:g.19369250G= NCBI36
NG_012795.1:g.56330C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.3477+181C= MANE Select ENSP00000269228.4:n.3477+181C=
ENST00000269228.9:c.3477+181C= ENSP00000269228.4:n.3477+181C=
ENST00000586150.5:c.232+181C=
ENST00000588867.1:n.232+181C=
ENST00000591051.1:c.2555+181C=
ENST00000591107.6:c.154+181C=
NM_000271.4:c.3477+181C= NP_000262.2:n.3477+181C=
XM_005258277.1:c.3528+181C= XP_005258334.1:n.3528+181C=
XM_005258278.3:c.3528+181C= XP_005258335.1:n.3528+181C=
XM_005258279.1:c.3477+181C= XP_005258336.1:n.3477+181C=
XM_006722479.2:c.3528+181C= XP_006722542.1:n.3528+181C=
XM_011526015.1:c.3063+181C= XP_011524317.1:n.3063+181C=
XM_005258278.5:c.3528+181C= XP_005258335.1:n.3528+181C=
XM_005258279.2:c.3477+181C= XP_005258336.1:n.3477+181C=
XM_006722479.3:c.3528+181C= XP_006722542.1:n.3528+181C=
XM_017025784.1:c.3528+181C= XP_016881273.1:n.3528+181C=
XM_017025785.1:c.3528+181C= XP_016881274.1:n.3528+181C=
XM_017025786.1:c.3477+181C= XP_016881275.1:n.3477+181C=
XM_017025787.1:c.3477+181C= XP_016881276.1:n.3477+181C=
NM_000271.5:c.3477+181C= MANE Select NP_000262.2:n.3477+181C=