Canonical Allele Identifier: CA913014997

Gene: NPC1

Linked Data

• MyVariant Identifiers: chr18:g.21148814dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23568850dup , CM000680.2:g.23568850dup	GRCh38
NC_000018.9:g.21148814dup , CM000680.1:g.21148814dup	GRCh37
NC_000018.8:g.19402812dup	NCBI36
NG_012795.1:g.22768dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.436dup MANE Select	ENSP00000269228.4:p.Tyr146LeufsTer24
ENST00000269228.9:c.436dup	ENSP00000269228.4:p.Tyr146LeufsTer24
ENST00000540608.5:n.350dup
NM_000271.4:c.436dup	NP_000262.2:p.Tyr146LeufsTer24
XM_005258277.1:c.436dup	XP_005258334.1:p.Tyr146LeufsTer24
XM_005258278.3:c.436dup	XP_005258335.1:p.Tyr146LeufsTer24
XM_005258279.1:c.436dup	XP_005258336.1:p.Tyr146LeufsTer24
XM_006722479.2:c.436dup	XP_006722542.1:p.Tyr146LeufsTer24
XM_011526015.1:c.-30dup	XP_011524317.1:n.-30dup
XM_005258278.5:c.436dup	XP_005258335.1:p.Tyr146LeufsTer24
XM_005258279.2:c.436dup	XP_005258336.1:p.Tyr146LeufsTer24
XM_006722479.3:c.436dup	XP_006722542.1:p.Tyr146LeufsTer24
XM_017025784.1:c.436dup	XP_016881273.1:p.Tyr146LeufsTer24
XM_017025785.1:c.436dup	XP_016881274.1:p.Tyr146LeufsTer24
XM_017025786.1:c.436dup	XP_016881275.1:p.Tyr146LeufsTer24
XM_017025787.1:c.436dup	XP_016881276.1:p.Tyr146LeufsTer24
NM_000271.5:c.436dup MANE Select	NP_000262.2:p.Tyr146LeufsTer24