Canonical Allele Identifier: CA401777571
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23556347G>A , CM000680.2:g.23556347G>A GRCh38
NC_000018.9:g.21136311G>A , CM000680.1:g.21136311G>A GRCh37
NC_000018.8:g.19390309G>A NCBI36
NG_012795.1:g.35271C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.1222C>T MANE Select ENSP00000269228.4:p.Leu408Phe
ENST00000269228.9:c.1222C>T ENSP00000269228.4:p.Leu408Phe
ENST00000540608.5:n.1136C>T
ENST00000591051.1:c.504C>T
NM_000271.4:c.1222C>T NP_000262.2:p.Leu408Phe
XM_005258277.1:c.1273C>T XP_005258334.1:p.Leu425Phe
XM_005258278.3:c.1273C>T XP_005258335.1:p.Leu425Phe
XM_005258279.1:c.1222C>T XP_005258336.1:p.Leu408Phe
XM_006722479.2:c.1273C>T XP_006722542.1:p.Leu425Phe
XM_011526015.1:c.808C>T XP_011524317.1:p.Leu270Phe
XM_005258278.5:c.1273C>T XP_005258335.1:p.Leu425Phe
XM_005258279.2:c.1222C>T XP_005258336.1:p.Leu408Phe
XM_006722479.3:c.1273C>T XP_006722542.1:p.Leu425Phe
XM_017025784.1:c.1273C>T XP_016881273.1:p.Leu425Phe
XM_017025785.1:c.1273C>T XP_016881274.1:p.Leu425Phe
XM_017025786.1:c.1222C>T XP_016881275.1:p.Leu408Phe
XM_017025787.1:c.1222C>T XP_016881276.1:p.Leu408Phe
NM_000271.5:c.1222C>T MANE Select NP_000262.2:p.Leu408Phe