Canonical Allele Identifier: CA401791064
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23534541C>G , CM000680.2:g.23534541C>G GRCh38
NC_000018.9:g.21114505C>G , CM000680.1:g.21114505C>G GRCh37
NC_000018.8:g.19368503C>G NCBI36
NG_012795.1:g.57077G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000271.5:c.3496G>C MANE Select NP_000262.2:p.Glu1166Gln
ENST00000269228.10:c.3496G>C MANE Select ENSP00000269228.4:p.Glu1166Gln
NM_000271.4:c.3496G>C NP_000262.2:p.Glu1166Gln
ENST00000269228.9:c.3496G>C ENSP00000269228.4:p.Glu1166Gln
ENST00000586150.5:c.251G>C
ENST00000587163.1:n.20G>C
ENST00000588867.1:n.251G>C
ENST00000591051.1:c.2574G>C
ENST00000591107.6:c.173G>C
XM_005258277.1:c.3547G>C XP_005258334.1:p.Glu1183Gln
XM_005258278.3:c.3547G>C XP_005258335.1:p.Glu1183Gln
XM_005258278.5:c.3547G>C XP_005258335.1:p.Glu1183Gln
XM_005258279.1:c.3496G>C XP_005258336.1:p.Glu1166Gln
XM_005258279.2:c.3496G>C XP_005258336.1:p.Glu1166Gln
XM_006722479.2:c.3547G>C XP_006722542.1:p.Glu1183Gln
XM_006722479.3:c.3547G>C XP_006722542.1:p.Glu1183Gln
XM_011526015.1:c.3082G>C XP_011524317.1:p.Glu1028Gln
XM_017025784.1:c.3547G>C XP_016881273.1:p.Glu1183Gln
XM_017025785.1:c.3547G>C XP_016881274.1:p.Glu1183Gln
XM_017025786.1:c.3496G>C XP_016881275.1:p.Glu1166Gln
XM_017025787.1:c.3496G>C XP_016881276.1:p.Glu1166Gln