Canonical Allele Identifier: CA2290163809
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23535412C= , CM000680.2:g.23535412C= GRCh38
NC_000018.9:g.21115376C= , CM000680.1:g.21115376C= GRCh37
NC_000018.8:g.19369374C= NCBI36
NG_012795.1:g.56206G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.3477+57G= MANE Select ENSP00000269228.4:n.3477+57G=
ENST00000269228.9:c.3477+57G= ENSP00000269228.4:n.3477+57G=
ENST00000586150.5:c.232+57G=
ENST00000588867.1:n.232+57G=
ENST00000591051.1:c.2555+57G=
ENST00000591107.6:c.154+57G=
NM_000271.4:c.3477+57G= NP_000262.2:n.3477+57G=
XM_005258277.1:c.3528+57G= XP_005258334.1:n.3528+57G=
XM_005258278.3:c.3528+57G= XP_005258335.1:n.3528+57G=
XM_005258279.1:c.3477+57G= XP_005258336.1:n.3477+57G=
XM_006722479.2:c.3528+57G= XP_006722542.1:n.3528+57G=
XM_011526015.1:c.3063+57G= XP_011524317.1:n.3063+57G=
XM_005258278.5:c.3528+57G= XP_005258335.1:n.3528+57G=
XM_005258279.2:c.3477+57G= XP_005258336.1:n.3477+57G=
XM_006722479.3:c.3528+57G= XP_006722542.1:n.3528+57G=
XM_017025784.1:c.3528+57G= XP_016881273.1:n.3528+57G=
XM_017025785.1:c.3528+57G= XP_016881274.1:n.3528+57G=
XM_017025786.1:c.3477+57G= XP_016881275.1:n.3477+57G=
XM_017025787.1:c.3477+57G= XP_016881276.1:n.3477+57G=
NM_000271.5:c.3477+57G= MANE Select NP_000262.2:n.3477+57G=