Canonical Allele Identifier: CA401776988

Gene: NPC1

Linked Data

• MyVariant Identifiers: chr18:g.21136207C>A (hg19) ; chr18:g.23556243C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23556243C>A , CM000680.2:g.23556243C>A	GRCh38
NC_000018.9:g.21136207C>A , CM000680.1:g.21136207C>A	GRCh37
NC_000018.8:g.19390205C>A	NCBI36
NG_012795.1:g.35375G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.1326G>T MANE Select	ENSP00000269228.4:p.Gln442His
ENST00000269228.9:c.1326G>T	ENSP00000269228.4:p.Gln442His
ENST00000540608.5:n.1240G>T
ENST00000591051.1:c.608G>T
NM_000271.4:c.1326G>T	NP_000262.2:p.Gln442His
XM_005258277.1:c.1377G>T	XP_005258334.1:p.Gln459His
XM_005258278.3:c.1377G>T	XP_005258335.1:p.Gln459His
XM_005258279.1:c.1326G>T	XP_005258336.1:p.Gln442His
XM_006722479.2:c.1377G>T	XP_006722542.1:p.Gln459His
XM_011526015.1:c.912G>T	XP_011524317.1:p.Gln304His
XM_005258278.5:c.1377G>T	XP_005258335.1:p.Gln459His
XM_005258279.2:c.1326G>T	XP_005258336.1:p.Gln442His
XM_006722479.3:c.1377G>T	XP_006722542.1:p.Gln459His
XM_017025784.1:c.1377G>T	XP_016881273.1:p.Gln459His
XM_017025785.1:c.1377G>T	XP_016881274.1:p.Gln459His
XM_017025786.1:c.1326G>T	XP_016881275.1:p.Gln442His
XM_017025787.1:c.1326G>T	XP_016881276.1:p.Gln442His
NM_000271.5:c.1326G>T MANE Select	NP_000262.2:p.Gln442His