Canonical Allele Identifier: CA401793196
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23540508G>C , CM000680.2:g.23540508G>C GRCh38
NC_000018.9:g.21120472G>C , CM000680.1:g.21120472G>C GRCh37
NC_000018.8:g.19374470G>C NCBI36
NG_012795.1:g.51110C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.2544C>G MANE Select ENSP00000269228.4:p.Phe848Leu
ENST00000269228.9:c.2544C>G ENSP00000269228.4:p.Phe848Leu
ENST00000540608.5:n.2458C>G
ENST00000586718.1:n.335C>G
ENST00000591051.1:c.1622C>G
NM_000271.4:c.2544C>G NP_000262.2:p.Phe848Leu
XM_005258277.1:c.2595C>G XP_005258334.1:p.Phe865Leu
XM_005258278.3:c.2595C>G XP_005258335.1:p.Phe865Leu
XM_005258279.1:c.2544C>G XP_005258336.1:p.Phe848Leu
XM_006722479.2:c.2595C>G XP_006722542.1:p.Phe865Leu
XM_011526015.1:c.2130C>G XP_011524317.1:p.Phe710Leu
XM_005258278.5:c.2595C>G XP_005258335.1:p.Phe865Leu
XM_005258279.2:c.2544C>G XP_005258336.1:p.Phe848Leu
XM_006722479.3:c.2595C>G XP_006722542.1:p.Phe865Leu
XM_017025784.1:c.2595C>G XP_016881273.1:p.Phe865Leu
XM_017025785.1:c.2595C>G XP_016881274.1:p.Phe865Leu
XM_017025786.1:c.2544C>G XP_016881275.1:p.Phe848Leu
XM_017025787.1:c.2544C>G XP_016881276.1:p.Phe848Leu
NM_000271.5:c.2544C>G MANE Select NP_000262.2:p.Phe848Leu