Canonical Allele Identifier: CA8913677

Gene: NPC1

Linked Data

• dbSNP Id: rs745647675
• ExAC: 18:21140455 G / T
• gnomAD v2: 18-21140455-G-T
• gnomAD v4: 18-23560491-G-T
• MyVariant Identifiers: chr18:g.21140455G>T (hg19) ; chr18:g.23560491G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23560491G>T , CM000680.2:g.23560491G>T	GRCh38
NC_000018.9:g.21140455G>T , CM000680.1:g.21140455G>T	GRCh37
NC_000018.8:g.19394453G>T	NCBI36
NG_012795.1:g.31127C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.632-11C>A MANE Select	ENSP00000269228.4:n.632-11C>A
ENST00000269228.9:c.632-11C>A	ENSP00000269228.4:n.632-11C>A
ENST00000540608.5:n.546-11C>A
NM_000271.4:c.632-11C>A	NP_000262.2:n.632-11C>A
XM_005258277.1:c.632-11C>A	XP_005258334.1:n.632-11C>A
XM_005258278.3:c.632-11C>A	XP_005258335.1:n.632-11C>A
XM_005258279.1:c.632-11C>A	XP_005258336.1:n.632-11C>A
XM_006722479.2:c.632-11C>A	XP_006722542.1:n.632-11C>A
XM_011526015.1:c.167-11C>A	XP_011524317.1:n.167-11C>A
XM_005258278.5:c.632-11C>A	XP_005258335.1:n.632-11C>A
XM_005258279.2:c.632-11C>A	XP_005258336.1:n.632-11C>A
XM_006722479.3:c.632-11C>A	XP_006722542.1:n.632-11C>A
XM_017025784.1:c.632-11C>A	XP_016881273.1:n.632-11C>A
XM_017025785.1:c.632-11C>A	XP_016881274.1:n.632-11C>A
XM_017025786.1:c.632-11C>A	XP_016881275.1:n.632-11C>A
XM_017025787.1:c.632-11C>A	XP_016881276.1:n.632-11C>A
NM_000271.5:c.632-11C>A MANE Select	NP_000262.2:n.632-11C>A