Canonical Allele Identifier: CA913014995
Gene: NPC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.21119886dup (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23539922dup , CM000680.2:g.23539922dup GRCh38
NC_000018.9:g.21119886dup , CM000680.1:g.21119886dup GRCh37
NC_000018.8:g.19373884dup NCBI36
NG_012795.1:g.51697dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.2685dup MANE Select ENSP00000269228.4:p.Gly896ArgfsTer22
ENST00000269228.9:c.2685dup ENSP00000269228.4:p.Gly896ArgfsTer22
ENST00000540608.5:n.2599dup
ENST00000586718.1:n.476dup
ENST00000591051.1:c.1763dup
NM_000271.4:c.2685dup NP_000262.2:p.Gly896ArgfsTer22
XM_005258277.1:c.2736dup XP_005258334.1:p.Gly913ArgfsTer22
XM_005258278.3:c.2736dup XP_005258335.1:p.Gly913ArgfsTer22
XM_005258279.1:c.2685dup XP_005258336.1:p.Gly896ArgfsTer22
XM_006722479.2:c.2736dup XP_006722542.1:p.Gly913ArgfsTer22
XM_011526015.1:c.2271dup XP_011524317.1:p.Gly758ArgfsTer22
XM_005258278.5:c.2736dup XP_005258335.1:p.Gly913ArgfsTer22
XM_005258279.2:c.2685dup XP_005258336.1:p.Gly896ArgfsTer22
XM_006722479.3:c.2736dup XP_006722542.1:p.Gly913ArgfsTer22
XM_017025784.1:c.2736dup XP_016881273.1:p.Gly913ArgfsTer22
XM_017025785.1:c.2736dup XP_016881274.1:p.Gly913ArgfsTer22
XM_017025786.1:c.2685dup XP_016881275.1:p.Gly896ArgfsTer22
XM_017025787.1:c.2685dup XP_016881276.1:p.Gly896ArgfsTer22
NM_000271.5:c.2685dup MANE Select NP_000262.2:p.Gly896ArgfsTer22