Canonical Allele Identifier: CA401785181
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23568891G>A , CM000680.2:g.23568891G>A GRCh38
NC_000018.9:g.21148855G>A , CM000680.1:g.21148855G>A GRCh37
NC_000018.8:g.19402853G>A NCBI36
NG_012795.1:g.22727C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.395C>T MANE Select ENSP00000269228.4:p.Pro132Leu
ENST00000269228.9:c.395C>T ENSP00000269228.4:p.Pro132Leu
ENST00000540608.5:n.309C>T
NM_000271.4:c.395C>T NP_000262.2:p.Pro132Leu
XM_005258277.1:c.395C>T XP_005258334.1:p.Pro132Leu
XM_005258278.3:c.395C>T XP_005258335.1:p.Pro132Leu
XM_005258279.1:c.395C>T XP_005258336.1:p.Pro132Leu
XM_006722479.2:c.395C>T XP_006722542.1:p.Pro132Leu
XM_011526015.1:c.-71C>T XP_011524317.1:n.-71C>T
XM_005258278.5:c.395C>T XP_005258335.1:p.Pro132Leu
XM_005258279.2:c.395C>T XP_005258336.1:p.Pro132Leu
XM_006722479.3:c.395C>T XP_006722542.1:p.Pro132Leu
XM_017025784.1:c.395C>T XP_016881273.1:p.Pro132Leu
XM_017025785.1:c.395C>T XP_016881274.1:p.Pro132Leu
XM_017025786.1:c.395C>T XP_016881275.1:p.Pro132Leu
XM_017025787.1:c.395C>T XP_016881276.1:p.Pro132Leu
NM_000271.5:c.395C>T MANE Select NP_000262.2:p.Pro132Leu