Canonical Allele Identifier: CA2695227443

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23539828dup , CM000680.2:g.23539828dup	GRCh38
NC_000018.9:g.21119792dup , CM000680.1:g.21119792dup	GRCh37
NC_000018.8:g.19373790dup	NCBI36
NG_012795.1:g.51791dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.2779dup MANE Select	ENSP00000269228.4:p.Ala927GlyfsTer?
ENST00000269228.9:c.2779dup	ENSP00000269228.4:p.Ala927GlyfsTer?
ENST00000540608.5:n.2693dup
ENST00000586718.1:n.570dup
ENST00000591051.1:c.1857dup
ENST00000591075.1:n.72dup
NM_000271.4:c.2779dup	NP_000262.2:p.Ala927GlyfsTer?
XM_005258277.1:c.2830dup	XP_005258334.1:p.Ala944GlyfsTer?
XM_005258278.3:c.2830dup	XP_005258335.1:p.Ala944GlyfsTer?
XM_005258279.1:c.2779dup	XP_005258336.1:p.Ala927GlyfsTer?
XM_006722479.2:c.2830dup	XP_006722542.1:p.Ala944GlyfsTer?
XM_011526015.1:c.2365dup	XP_011524317.1:p.Ala789GlyfsTer?
XM_005258278.5:c.2830dup	XP_005258335.1:p.Ala944GlyfsTer?
XM_005258279.2:c.2779dup	XP_005258336.1:p.Ala927GlyfsTer?
XM_006722479.3:c.2830dup	XP_006722542.1:p.Ala944GlyfsTer?
XM_017025784.1:c.2830dup	XP_016881273.1:p.Ala944GlyfsTer?
XM_017025785.1:c.2830dup	XP_016881274.1:p.Ala944GlyfsTer?
XM_017025786.1:c.2779dup	XP_016881275.1:p.Ala927GlyfsTer?
XM_017025787.1:c.2779dup	XP_016881276.1:p.Ala927GlyfsTer?
NM_000271.5:c.2779dup MANE Select	NP_000262.2:p.Ala927GlyfsTer?