Canonical Allele Identifier: CA503322069

Gene: NPC1

Linked Data

• MyVariant Identifiers: chr18:g.21113437C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23533473C>A , CM000680.2:g.23533473C>A	GRCh38
NC_000018.9:g.21113437C>A , CM000680.1:g.21113437C>A	GRCh37
NC_000018.8:g.19367435C>A	NCBI36
NG_012795.1:g.58145G>T
NG_033119.1:g.35004C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.3636G>T MANE Select	ENSP00000269228.4:p.Val1212=
ENST00000269228.9:c.3636G>T	ENSP00000269228.4:p.Val1212=
ENST00000586150.5:c.391G>T
ENST00000587163.1:n.160G>T
ENST00000588867.1:n.1319G>T
ENST00000590723.5:c.45G>T	ENSP00000464755.1:p.Val15=
ENST00000591051.1:c.2714G>T
ENST00000591107.6:c.313G>T
NM_000271.4:c.3636G>T	NP_000262.2:p.Val1212=
XM_005258277.1:c.3687G>T	XP_005258334.1:p.Val1229=
XM_005258278.3:c.3687G>T	XP_005258335.1:p.Val1229=
XM_005258279.1:c.3636G>T	XP_005258336.1:p.Val1212=
XM_006722479.2:c.3687G>T	XP_006722542.1:p.Val1229=
XM_011526015.1:c.3222G>T	XP_011524317.1:p.Val1074=
XM_005258278.5:c.3687G>T	XP_005258335.1:p.Val1229=
XM_005258279.2:c.3636G>T	XP_005258336.1:p.Val1212=
XM_006722479.3:c.3687G>T	XP_006722542.1:p.Val1229=
XM_017025784.1:c.3687G>T	XP_016881273.1:p.Val1229=
XM_017025785.1:c.3687G>T	XP_016881274.1:p.Val1229=
XM_017025786.1:c.3636G>T	XP_016881275.1:p.Val1212=
XM_017025787.1:c.3636G>T	XP_016881276.1:p.Val1212=
NM_000271.5:c.3636G>T MANE Select	NP_000262.2:p.Val1212=