Canonical Allele Identifier: CA297084875

Gene: NPC1

Linked Data

• dbSNP Id: rs2516343
• MyVariant Identifiers: chr18:g.21162278A>G (hg19) ; chr18:g.23582314A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23582314A>G , CM000680.2:g.23582314A>G	GRCh38
NC_000018.9:g.21162278A>G , CM000680.1:g.21162278A>G	GRCh37
NC_000018.8:g.19416276A>G	NCBI36
NG_012795.1:g.9304T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.57+3973T>C MANE Select	ENSP00000269228.4:n.57+3973T>C
ENST00000269228.9:c.57+3973T>C	ENSP00000269228.4:n.57+3973T>C
ENST00000540608.5:n.201+3973T>C
NM_000271.4:c.57+3973T>C	NP_000262.2:n.57+3973T>C
XM_005258277.1:c.57+3973T>C	XP_005258334.1:n.57+3973T>C
XM_005258278.3:c.57+3973T>C	XP_005258335.1:n.57+3973T>C
XM_005258279.1:c.57+3973T>C	XP_005258336.1:n.57+3973T>C
XM_006722479.2:c.57+3973T>C	XP_006722542.1:n.57+3973T>C
XM_005258278.5:c.57+3973T>C	XP_005258335.1:n.57+3973T>C
XM_005258279.2:c.57+3973T>C	XP_005258336.1:n.57+3973T>C
XM_006722479.3:c.57+3973T>C	XP_006722542.1:n.57+3973T>C
XM_017025784.1:c.57+3973T>C	XP_016881273.1:n.57+3973T>C
XM_017025785.1:c.57+3973T>C	XP_016881274.1:n.57+3973T>C
XM_017025786.1:c.57+3973T>C	XP_016881275.1:n.57+3973T>C
XM_017025787.1:c.57+3973T>C	XP_016881276.1:n.57+3973T>C
NM_000271.5:c.57+3973T>C MANE Select	NP_000262.2:n.57+3973T>C