Canonical Allele Identifier: CA401772132

Gene: NPC1

Linked Data

• ClinVar Variation Id: 553366
• ClinVar RCV Id: RCV000668796
• dbSNP Id: rs1555634690
• MyVariant Identifiers: chr18:g.21124923C>T (hg19) ; chr18:g.23544959C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23544959C>T , CM000680.2:g.23544959C>T	GRCh38
NC_000018.9:g.21124923C>T , CM000680.1:g.21124923C>T	GRCh37
NC_000018.8:g.19378921C>T	NCBI36
NG_012795.1:g.46659G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.1947+1G>A MANE Select	ENSP00000269228.4:n.1947+1G>A
ENST00000269228.9:c.1947+1G>A	ENSP00000269228.4:n.1947+1G>A
ENST00000540608.5:n.1861+1G>A
ENST00000591051.1:c.1025+1G>A
NM_000271.4:c.1947+1G>A	NP_000262.2:n.1947+1G>A
XM_005258277.1:c.1998+1G>A	XP_005258334.1:n.1998+1G>A
XM_005258278.3:c.1998+1G>A	XP_005258335.1:n.1998+1G>A
XM_005258279.1:c.1947+1G>A	XP_005258336.1:n.1947+1G>A
XM_006722479.2:c.1998+1G>A	XP_006722542.1:n.1998+1G>A
XM_011526015.1:c.1533+1G>A	XP_011524317.1:n.1533+1G>A
XM_005258278.5:c.1998+1G>A	XP_005258335.1:n.1998+1G>A
XM_005258279.2:c.1947+1G>A	XP_005258336.1:n.1947+1G>A
XM_006722479.3:c.1998+1G>A	XP_006722542.1:n.1998+1G>A
XM_017025784.1:c.1998+1G>A	XP_016881273.1:n.1998+1G>A
XM_017025785.1:c.1998+1G>A	XP_016881274.1:n.1998+1G>A
XM_017025786.1:c.1947+1G>A	XP_016881275.1:n.1947+1G>A
XM_017025787.1:c.1947+1G>A	XP_016881276.1:n.1947+1G>A
NM_000271.5:c.1947+1G>A MANE Select	NP_000262.2:n.1947+1G>A