Canonical Allele Identifier: CA503521762

Gene: NPC1

Linked Data

• MyVariant Identifiers: chr18:g.21115616A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23535652A>C , CM000680.2:g.23535652A>C	GRCh38
NC_000018.9:g.21115616A>C , CM000680.1:g.21115616A>C	GRCh37
NC_000018.8:g.19369614A>C	NCBI36
NG_012795.1:g.55966T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.3294T>G MANE Select	ENSP00000269228.4:p.Thr1098=
ENST00000269228.9:c.3294T>G	ENSP00000269228.4:p.Thr1098=
ENST00000586150.5:c.49T>G
ENST00000588867.1:n.49T>G
ENST00000591051.1:c.2372T>G
NM_000271.4:c.3294T>G	NP_000262.2:p.Thr1098=
XM_005258277.1:c.3345T>G	XP_005258334.1:p.Thr1115=
XM_005258278.3:c.3345T>G	XP_005258335.1:p.Thr1115=
XM_005258279.1:c.3294T>G	XP_005258336.1:p.Thr1098=
XM_006722479.2:c.3345T>G	XP_006722542.1:p.Thr1115=
XM_011526015.1:c.2880T>G	XP_011524317.1:p.Thr960=
XM_005258278.5:c.3345T>G	XP_005258335.1:p.Thr1115=
XM_005258279.2:c.3294T>G	XP_005258336.1:p.Thr1098=
XM_006722479.3:c.3345T>G	XP_006722542.1:p.Thr1115=
XM_017025784.1:c.3345T>G	XP_016881273.1:p.Thr1115=
XM_017025785.1:c.3345T>G	XP_016881274.1:p.Thr1115=
XM_017025786.1:c.3294T>G	XP_016881275.1:p.Thr1098=
XM_017025787.1:c.3294T>G	XP_016881276.1:p.Thr1098=
NM_000271.5:c.3294T>G MANE Select	NP_000262.2:p.Thr1098=