Canonical Allele Identifier: CA401791139

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23535479T>G , CM000680.2:g.23535479T>G	GRCh38
NC_000018.9:g.21115443T>G , CM000680.1:g.21115443T>G	GRCh37
NC_000018.8:g.19369441T>G	NCBI36
NG_012795.1:g.56139A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000271.5:c.3467A>C MANE Select	NP_000262.2:p.Asn1156Thr
ENST00000269228.10:c.3467A>C MANE Select	ENSP00000269228.4:p.Asn1156Thr
NM_000271.4:c.3467A>C	NP_000262.2:p.Asn1156Thr
ENST00000269228.9:c.3467A>C	ENSP00000269228.4:p.Asn1156Thr
ENST00000586150.5:c.222A>C
ENST00000588867.1:n.222A>C
ENST00000591051.1:c.2545A>C
ENST00000591107.6:c.144A>C
XM_005258277.1:c.3518A>C	XP_005258334.1:p.Asn1173Thr
XM_005258278.3:c.3518A>C	XP_005258335.1:p.Asn1173Thr
XM_005258278.5:c.3518A>C	XP_005258335.1:p.Asn1173Thr
XM_005258279.1:c.3467A>C	XP_005258336.1:p.Asn1156Thr
XM_005258279.2:c.3467A>C	XP_005258336.1:p.Asn1156Thr
XM_006722479.2:c.3518A>C	XP_006722542.1:p.Asn1173Thr
XM_006722479.3:c.3518A>C	XP_006722542.1:p.Asn1173Thr
XM_011526015.1:c.3053A>C	XP_011524317.1:p.Asn1018Thr
XM_017025784.1:c.3518A>C	XP_016881273.1:p.Asn1173Thr
XM_017025785.1:c.3518A>C	XP_016881274.1:p.Asn1173Thr
XM_017025786.1:c.3467A>C	XP_016881275.1:p.Asn1156Thr
XM_017025787.1:c.3467A>C	XP_016881276.1:p.Asn1156Thr