Canonical Allele Identifier: CA401781438

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23560468T>A , CM000680.2:g.23560468T>A	GRCh38
NC_000018.9:g.21140432T>A , CM000680.1:g.21140432T>A	GRCh37
NC_000018.8:g.19394430T>A	NCBI36
NG_012795.1:g.31150A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000271.5:c.644A>T MANE Select	NP_000262.2:p.His215Leu
ENST00000269228.10:c.644A>T MANE Select	ENSP00000269228.4:p.His215Leu
NM_000271.4:c.644A>T	NP_000262.2:p.His215Leu
ENST00000269228.9:c.644A>T	ENSP00000269228.4:p.His215Leu
ENST00000540608.5:n.558A>T
XM_005258277.1:c.644A>T	XP_005258334.1:p.His215Leu
XM_005258278.3:c.644A>T	XP_005258335.1:p.His215Leu
XM_005258278.5:c.644A>T	XP_005258335.1:p.His215Leu
XM_005258279.1:c.644A>T	XP_005258336.1:p.His215Leu
XM_005258279.2:c.644A>T	XP_005258336.1:p.His215Leu
XM_006722479.2:c.644A>T	XP_006722542.1:p.His215Leu
XM_006722479.3:c.644A>T	XP_006722542.1:p.His215Leu
XM_011526015.1:c.179A>T	XP_011524317.1:p.His60Leu
XM_017025784.1:c.644A>T	XP_016881273.1:p.His215Leu
XM_017025785.1:c.644A>T	XP_016881274.1:p.His215Leu
XM_017025786.1:c.644A>T	XP_016881275.1:p.His215Leu
XM_017025787.1:c.644A>T	XP_016881276.1:p.His215Leu