Canonical Allele Identifier: CA503521744

Gene: NPC1

Linked Data

• MyVariant Identifiers: chr18:g.21115595G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23535631G>C , CM000680.2:g.23535631G>C	GRCh38
NC_000018.9:g.21115595G>C , CM000680.1:g.21115595G>C	GRCh37
NC_000018.8:g.19369593G>C	NCBI36
NG_012795.1:g.55987C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.3315C>G MANE Select	ENSP00000269228.4:p.Ser1105=
ENST00000269228.9:c.3315C>G	ENSP00000269228.4:p.Ser1105=
ENST00000586150.5:c.70C>G
ENST00000588867.1:n.70C>G
ENST00000591051.1:c.2393C>G
NM_000271.4:c.3315C>G	NP_000262.2:p.Ser1105=
XM_005258277.1:c.3366C>G	XP_005258334.1:p.Ser1122=
XM_005258278.3:c.3366C>G	XP_005258335.1:p.Ser1122=
XM_005258279.1:c.3315C>G	XP_005258336.1:p.Ser1105=
XM_006722479.2:c.3366C>G	XP_006722542.1:p.Ser1122=
XM_011526015.1:c.2901C>G	XP_011524317.1:p.Ser967=
XM_005258278.5:c.3366C>G	XP_005258335.1:p.Ser1122=
XM_005258279.2:c.3315C>G	XP_005258336.1:p.Ser1105=
XM_006722479.3:c.3366C>G	XP_006722542.1:p.Ser1122=
XM_017025784.1:c.3366C>G	XP_016881273.1:p.Ser1122=
XM_017025785.1:c.3366C>G	XP_016881274.1:p.Ser1122=
XM_017025786.1:c.3315C>G	XP_016881275.1:p.Ser1105=
XM_017025787.1:c.3315C>G	XP_016881276.1:p.Ser1105=
NM_000271.5:c.3315C>G MANE Select	NP_000262.2:p.Ser1105=