Canonical Allele Identifier: CA401778286

Gene: NPC1

Linked Data

• dbSNP Id: rs1257680553
• gnomAD v2: 18-21136422-C-A
• gnomAD v4: 18-23556458-C-A
• MyVariant Identifiers: chr18:g.21136422C>A (hg19) ; chr18:g.23556458C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.1111G>T MANE Select	ENSP00000269228.4:p.Val371Phe
ENST00000269228.9:c.1111G>T	ENSP00000269228.4:p.Val371Phe
ENST00000540608.5:n.1025G>T
ENST00000591051.1:c.393G>T
NM_000271.4:c.1111G>T	NP_000262.2:p.Val371Phe
XM_005258277.1:c.1162G>T	XP_005258334.1:p.Val388Phe
XM_005258278.3:c.1162G>T	XP_005258335.1:p.Val388Phe
XM_005258279.1:c.1111G>T	XP_005258336.1:p.Val371Phe
XM_006722479.2:c.1162G>T	XP_006722542.1:p.Val388Phe
XM_011526015.1:c.697G>T	XP_011524317.1:p.Val233Phe
XM_005258278.5:c.1162G>T	XP_005258335.1:p.Val388Phe
XM_005258279.2:c.1111G>T	XP_005258336.1:p.Val371Phe
XM_006722479.3:c.1162G>T	XP_006722542.1:p.Val388Phe
XM_017025784.1:c.1162G>T	XP_016881273.1:p.Val388Phe
XM_017025785.1:c.1162G>T	XP_016881274.1:p.Val388Phe
XM_017025786.1:c.1111G>T	XP_016881275.1:p.Val371Phe
XM_017025787.1:c.1111G>T	XP_016881276.1:p.Val371Phe
NM_000271.5:c.1111G>T MANE Select	NP_000262.2:p.Val371Phe