Canonical Allele Identifier: CA401792876

Gene: NPC1

Linked Data

• ClinVar Variation Id: 1072937
• ClinVar RCV Id: RCV001385787
• dbSNP Id: rs2145373524
• MyVariant Identifiers: chr18:g.21119887C>A (hg19) ; chr18:g.23539923C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23539923C>A , CM000680.2:g.23539923C>A	GRCh38
NC_000018.9:g.21119887C>A , CM000680.1:g.21119887C>A	GRCh37
NC_000018.8:g.19373885C>A	NCBI36
NG_012795.1:g.51695G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.2683G>T MANE Select	ENSP00000269228.4:p.Glu895Ter
ENST00000269228.9:c.2683G>T	ENSP00000269228.4:p.Glu895Ter
ENST00000540608.5:n.2597G>T
ENST00000586718.1:n.474G>T
ENST00000591051.1:c.1761G>T
NM_000271.4:c.2683G>T	NP_000262.2:p.Glu895Ter
XM_005258277.1:c.2734G>T	XP_005258334.1:p.Glu912Ter
XM_005258278.3:c.2734G>T	XP_005258335.1:p.Glu912Ter
XM_005258279.1:c.2683G>T	XP_005258336.1:p.Glu895Ter
XM_006722479.2:c.2734G>T	XP_006722542.1:p.Glu912Ter
XM_011526015.1:c.2269G>T	XP_011524317.1:p.Glu757Ter
XM_005258278.5:c.2734G>T	XP_005258335.1:p.Glu912Ter
XM_005258279.2:c.2683G>T	XP_005258336.1:p.Glu895Ter
XM_006722479.3:c.2734G>T	XP_006722542.1:p.Glu912Ter
XM_017025784.1:c.2734G>T	XP_016881273.1:p.Glu912Ter
XM_017025785.1:c.2734G>T	XP_016881274.1:p.Glu912Ter
XM_017025786.1:c.2683G>T	XP_016881275.1:p.Glu895Ter
XM_017025787.1:c.2683G>T	XP_016881276.1:p.Glu895Ter
NM_000271.5:c.2683G>T MANE Select	NP_000262.2:p.Glu895Ter