Canonical Allele Identifier: CA2290165959

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23539941C= , CM000680.2:g.23539941C=	GRCh38
NC_000018.9:g.21119905C= , CM000680.1:g.21119905C=	GRCh37
NC_000018.8:g.19373903C=	NCBI36
NG_012795.1:g.51677G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.2665G= MANE Select	ENSP00000269228.4:p.Val889=
ENST00000269228.9:c.2665G=	ENSP00000269228.4:p.Val889=
ENST00000540608.5:n.2579G=
ENST00000586718.1:n.456G=
ENST00000591051.1:c.1743G=
NM_000271.4:c.2665G=	NP_000262.2:p.Val889=
XM_005258277.1:c.2716G=	XP_005258334.1:p.Val906=
XM_005258278.3:c.2716G=	XP_005258335.1:p.Val906=
XM_005258279.1:c.2665G=	XP_005258336.1:p.Val889=
XM_006722479.2:c.2716G=	XP_006722542.1:p.Val906=
XM_011526015.1:c.2251G=	XP_011524317.1:p.Val751=
XM_005258278.5:c.2716G=	XP_005258335.1:p.Val906=
XM_005258279.2:c.2665G=	XP_005258336.1:p.Val889=
XM_006722479.3:c.2716G=	XP_006722542.1:p.Val906=
XM_017025784.1:c.2716G=	XP_016881273.1:p.Val906=
XM_017025785.1:c.2716G=	XP_016881274.1:p.Val906=
XM_017025786.1:c.2665G=	XP_016881275.1:p.Val889=
XM_017025787.1:c.2665G=	XP_016881276.1:p.Val889=
NM_000271.5:c.2665G= MANE Select	NP_000262.2:p.Val889=