Canonical Allele Identifier: CA401793216
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23540519C>G , CM000680.2:g.23540519C>G GRCh38
NC_000018.9:g.21120483C>G , CM000680.1:g.21120483C>G GRCh37
NC_000018.8:g.19374481C>G NCBI36
NG_012795.1:g.51099G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.2533G>C MANE Select ENSP00000269228.4:p.Val845Leu
ENST00000269228.9:c.2533G>C ENSP00000269228.4:p.Val845Leu
ENST00000540608.5:n.2447G>C
ENST00000586718.1:n.324G>C
ENST00000591051.1:c.1611G>C
NM_000271.4:c.2533G>C NP_000262.2:p.Val845Leu
XM_005258277.1:c.2584G>C XP_005258334.1:p.Val862Leu
XM_005258278.3:c.2584G>C XP_005258335.1:p.Val862Leu
XM_005258279.1:c.2533G>C XP_005258336.1:p.Val845Leu
XM_006722479.2:c.2584G>C XP_006722542.1:p.Val862Leu
XM_011526015.1:c.2119G>C XP_011524317.1:p.Val707Leu
XM_005258278.5:c.2584G>C XP_005258335.1:p.Val862Leu
XM_005258279.2:c.2533G>C XP_005258336.1:p.Val845Leu
XM_006722479.3:c.2584G>C XP_006722542.1:p.Val862Leu
XM_017025784.1:c.2584G>C XP_016881273.1:p.Val862Leu
XM_017025785.1:c.2584G>C XP_016881274.1:p.Val862Leu
XM_017025786.1:c.2533G>C XP_016881275.1:p.Val845Leu
XM_017025787.1:c.2533G>C XP_016881276.1:p.Val845Leu
NM_000271.5:c.2533G>C MANE Select NP_000262.2:p.Val845Leu