Canonical Allele Identifier: CA401778289

Gene: NPC1

Linked Data

• MyVariant Identifiers: chr18:g.21136422C>T (hg19) ; chr18:g.23556458C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23556458C>T , CM000680.2:g.23556458C>T	GRCh38
NC_000018.9:g.21136422C>T , CM000680.1:g.21136422C>T	GRCh37
NC_000018.8:g.19390420C>T	NCBI36
NG_012795.1:g.35160G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.1111G>A MANE Select	ENSP00000269228.4:p.Val371Ile
ENST00000269228.9:c.1111G>A	ENSP00000269228.4:p.Val371Ile
ENST00000540608.5:n.1025G>A
ENST00000591051.1:c.393G>A
NM_000271.4:c.1111G>A	NP_000262.2:p.Val371Ile
XM_005258277.1:c.1162G>A	XP_005258334.1:p.Val388Ile
XM_005258278.3:c.1162G>A	XP_005258335.1:p.Val388Ile
XM_005258279.1:c.1111G>A	XP_005258336.1:p.Val371Ile
XM_006722479.2:c.1162G>A	XP_006722542.1:p.Val388Ile
XM_011526015.1:c.697G>A	XP_011524317.1:p.Val233Ile
XM_005258278.5:c.1162G>A	XP_005258335.1:p.Val388Ile
XM_005258279.2:c.1111G>A	XP_005258336.1:p.Val371Ile
XM_006722479.3:c.1162G>A	XP_006722542.1:p.Val388Ile
XM_017025784.1:c.1162G>A	XP_016881273.1:p.Val388Ile
XM_017025785.1:c.1162G>A	XP_016881274.1:p.Val388Ile
XM_017025786.1:c.1111G>A	XP_016881275.1:p.Val371Ile
XM_017025787.1:c.1111G>A	XP_016881276.1:p.Val371Ile
NM_000271.5:c.1111G>A MANE Select	NP_000262.2:p.Val371Ile