Canonical Allele Identifier: CA401777678
Gene: NPC1 HGNC NCBI

Linked Data

dbSNP Id: rs1415833171

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23556364A>G , CM000680.2:g.23556364A>G GRCh38
NC_000018.9:g.21136328A>G , CM000680.1:g.21136328A>G GRCh37
NC_000018.8:g.19390326A>G NCBI36
NG_012795.1:g.35254T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.1205T>C MANE Select ENSP00000269228.4:p.Phe402Ser
ENST00000269228.9:c.1205T>C ENSP00000269228.4:p.Phe402Ser
ENST00000540608.5:n.1119T>C
ENST00000591051.1:c.487T>C
NM_000271.4:c.1205T>C NP_000262.2:p.Phe402Ser
XM_005258277.1:c.1256T>C XP_005258334.1:p.Phe419Ser
XM_005258278.3:c.1256T>C XP_005258335.1:p.Phe419Ser
XM_005258279.1:c.1205T>C XP_005258336.1:p.Phe402Ser
XM_006722479.2:c.1256T>C XP_006722542.1:p.Phe419Ser
XM_011526015.1:c.791T>C XP_011524317.1:p.Phe264Ser
XM_005258278.5:c.1256T>C XP_005258335.1:p.Phe419Ser
XM_005258279.2:c.1205T>C XP_005258336.1:p.Phe402Ser
XM_006722479.3:c.1256T>C XP_006722542.1:p.Phe419Ser
XM_017025784.1:c.1256T>C XP_016881273.1:p.Phe419Ser
XM_017025785.1:c.1256T>C XP_016881274.1:p.Phe419Ser
XM_017025786.1:c.1205T>C XP_016881275.1:p.Phe402Ser
XM_017025787.1:c.1205T>C XP_016881276.1:p.Phe402Ser
NM_000271.5:c.1205T>C MANE Select NP_000262.2:p.Phe402Ser