Canonical Allele Identifier: CA297074790

Gene: NPC1

Linked Data

• ClinVar Variation Id: 1147420
• ClinVar RCV Id: RCV001486922
• dbSNP Id: rs952084518
• MyVariant Identifiers: chr18:g.21140454G>A (hg19) ; chr18:g.23560490G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23560490G>A , CM000680.2:g.23560490G>A	GRCh38
NC_000018.9:g.21140454G>A , CM000680.1:g.21140454G>A	GRCh37
NC_000018.8:g.19394452G>A	NCBI36
NG_012795.1:g.31128C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.632-10C>T MANE Select	ENSP00000269228.4:n.632-10C>T
ENST00000269228.9:c.632-10C>T	ENSP00000269228.4:n.632-10C>T
ENST00000540608.5:n.546-10C>T
NM_000271.4:c.632-10C>T	NP_000262.2:n.632-10C>T
XM_005258277.1:c.632-10C>T	XP_005258334.1:n.632-10C>T
XM_005258278.3:c.632-10C>T	XP_005258335.1:n.632-10C>T
XM_005258279.1:c.632-10C>T	XP_005258336.1:n.632-10C>T
XM_006722479.2:c.632-10C>T	XP_006722542.1:n.632-10C>T
XM_011526015.1:c.167-10C>T	XP_011524317.1:n.167-10C>T
XM_005258278.5:c.632-10C>T	XP_005258335.1:n.632-10C>T
XM_005258279.2:c.632-10C>T	XP_005258336.1:n.632-10C>T
XM_006722479.3:c.632-10C>T	XP_006722542.1:n.632-10C>T
XM_017025784.1:c.632-10C>T	XP_016881273.1:n.632-10C>T
XM_017025785.1:c.632-10C>T	XP_016881274.1:n.632-10C>T
XM_017025786.1:c.632-10C>T	XP_016881275.1:n.632-10C>T
XM_017025787.1:c.632-10C>T	XP_016881276.1:n.632-10C>T
NM_000271.5:c.632-10C>T MANE Select	NP_000262.2:n.632-10C>T