Canonical Allele Identifier: CA401792233

Gene: NPC1

Linked Data

• gnomAD v4: 18-23538615-G-T
• MyVariant Identifiers: chr18:g.21118579G>T (hg19) ; chr18:g.23538615G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23538615G>T , CM000680.2:g.23538615G>T	GRCh38
NC_000018.9:g.21118579G>T , CM000680.1:g.21118579G>T	GRCh37
NC_000018.8:g.19372577G>T	NCBI36
NG_012795.1:g.53003C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.2968C>A MANE Select	ENSP00000269228.4:p.Pro990Thr
ENST00000269228.9:c.2968C>A	ENSP00000269228.4:p.Pro990Thr
ENST00000591051.1:c.2046C>A
ENST00000591075.1:n.601C>A
ENST00000591955.1:n.311C>A
NM_000271.4:c.2968C>A	NP_000262.2:p.Pro990Thr
XM_005258277.1:c.3019C>A	XP_005258334.1:p.Pro1007Thr
XM_005258278.3:c.3019C>A	XP_005258335.1:p.Pro1007Thr
XM_005258279.1:c.2968C>A	XP_005258336.1:p.Pro990Thr
XM_006722479.2:c.3019C>A	XP_006722542.1:p.Pro1007Thr
XM_011526015.1:c.2554C>A	XP_011524317.1:p.Pro852Thr
XM_005258278.5:c.3019C>A	XP_005258335.1:p.Pro1007Thr
XM_005258279.2:c.2968C>A	XP_005258336.1:p.Pro990Thr
XM_006722479.3:c.3019C>A	XP_006722542.1:p.Pro1007Thr
XM_017025784.1:c.3019C>A	XP_016881273.1:p.Pro1007Thr
XM_017025785.1:c.3019C>A	XP_016881274.1:p.Pro1007Thr
XM_017025786.1:c.2968C>A	XP_016881275.1:p.Pro990Thr
XM_017025787.1:c.2968C>A	XP_016881276.1:p.Pro990Thr
NM_000271.5:c.2968C>A MANE Select	NP_000262.2:p.Pro990Thr