Canonical Allele Identifier: CA2290163949
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23535688G= , CM000680.2:g.23535688G= GRCh38
NC_000018.9:g.21115652G= , CM000680.1:g.21115652G= GRCh37
NC_000018.8:g.19369650G= NCBI36
NG_012795.1:g.55930C=

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.3258C= MANE Select ENSP00000269228.4:p.Val1086=
ENST00000269228.9:c.3258C= ENSP00000269228.4:p.Val1086=
ENST00000586150.5:c.13C=
ENST00000588867.1:n.13C=
ENST00000591051.1:c.2336C=
NM_000271.4:c.3258C= NP_000262.2:p.Val1086=
XM_005258277.1:c.3309C= XP_005258334.1:p.Val1103=
XM_005258278.3:c.3309C= XP_005258335.1:p.Val1103=
XM_005258279.1:c.3258C= XP_005258336.1:p.Val1086=
XM_006722479.2:c.3309C= XP_006722542.1:p.Val1103=
XM_011526015.1:c.2844C= XP_011524317.1:p.Val948=
XM_005258278.5:c.3309C= XP_005258335.1:p.Val1103=
XM_005258279.2:c.3258C= XP_005258336.1:p.Val1086=
XM_006722479.3:c.3309C= XP_006722542.1:p.Val1103=
XM_017025784.1:c.3309C= XP_016881273.1:p.Val1103=
XM_017025785.1:c.3309C= XP_016881274.1:p.Val1103=
XM_017025786.1:c.3258C= XP_016881275.1:p.Val1086=
XM_017025787.1:c.3258C= XP_016881276.1:p.Val1086=
NM_000271.5:c.3258C= MANE Select NP_000262.2:p.Val1086=