Canonical Allele Identifier: CA503321914

Gene: NPC1

Linked Data

• MyVariant Identifiers: chr18:g.21112244T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23532280T>G , CM000680.2:g.23532280T>G	GRCh38
NC_000018.9:g.21112244T>G , CM000680.1:g.21112244T>G	GRCh37
NC_000018.8:g.19366242T>G	NCBI36
NG_012795.1:g.59338A>C
NG_033119.1:g.33811T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269228.10:c.3759A>C MANE Select	ENSP00000269228.4:p.Pro1253=
ENST00000269228.9:c.3759A>C	ENSP00000269228.4:p.Pro1253=
ENST00000586150.5:c.509+1075A>C
ENST00000588867.1:n.1442A>C
ENST00000590723.5:c.163+1075A>C	ENSP00000464755.1:n.163+1075A>C
ENST00000591051.1:c.2837A>C
ENST00000591107.6:c.431+1075A>C
ENST00000593280.2:c.86+1075A>C
NM_000271.4:c.3759A>C	NP_000262.2:p.Pro1253=
XM_005258277.1:c.3805+1075A>C	XP_005258334.1:n.3805+1075A>C
XM_005258278.3:c.3810A>C	XP_005258335.1:p.Pro1270=
XM_005258279.1:c.3754+1075A>C	XP_005258336.1:n.3754+1075A>C
XM_006722479.2:c.3805+1075A>C	XP_006722542.1:n.3805+1075A>C
XM_011526015.1:c.3340+1075A>C	XP_011524317.1:n.3340+1075A>C
XM_005258278.5:c.3810A>C	XP_005258335.1:p.Pro1270=
XM_005258279.2:c.3754+1075A>C	XP_005258336.1:n.3754+1075A>C
XM_006722479.3:c.3805+1075A>C	XP_006722542.1:n.3805+1075A>C
XM_017025784.1:c.3805+1075A>C	XP_016881273.1:n.3805+1075A>C
XM_017025785.1:c.3805+1075A>C	XP_016881274.1:n.3805+1075A>C
XM_017025786.1:c.3754+1075A>C	XP_016881275.1:n.3754+1075A>C
XM_017025787.1:c.3754+1075A>C	XP_016881276.1:n.3754+1075A>C
NM_000271.5:c.3759A>C MANE Select	NP_000262.2:p.Pro1253=