Canonical Allele Identifier: CA2641274056
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23540152C>A , CM000680.2:g.23540152C>A GRCh38
NC_000018.9:g.21120116C>A , CM000680.1:g.21120116C>A GRCh37
NC_000018.8:g.19374114C>A NCBI36
NG_012795.1:g.51466G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.2605-151G>T MANE Select ENSP00000269228.4:n.2605-151G>T
ENST00000269228.9:c.2605-151G>T ENSP00000269228.4:n.2605-151G>T
ENST00000540608.5:n.2519-151G>T
ENST00000586718.1:n.396-151G>T
ENST00000591051.1:c.1683-151G>T
NM_000271.4:c.2605-151G>T NP_000262.2:n.2605-151G>T
XM_005258277.1:c.2656-151G>T XP_005258334.1:n.2656-151G>T
XM_005258278.3:c.2656-151G>T XP_005258335.1:n.2656-151G>T
XM_005258279.1:c.2605-151G>T XP_005258336.1:n.2605-151G>T
XM_006722479.2:c.2656-151G>T XP_006722542.1:n.2656-151G>T
XM_011526015.1:c.2191-151G>T XP_011524317.1:n.2191-151G>T
XM_005258278.5:c.2656-151G>T XP_005258335.1:n.2656-151G>T
XM_005258279.2:c.2605-151G>T XP_005258336.1:n.2605-151G>T
XM_006722479.3:c.2656-151G>T XP_006722542.1:n.2656-151G>T
XM_017025784.1:c.2656-151G>T XP_016881273.1:n.2656-151G>T
XM_017025785.1:c.2656-151G>T XP_016881274.1:n.2656-151G>T
XM_017025786.1:c.2605-151G>T XP_016881275.1:n.2605-151G>T
XM_017025787.1:c.2605-151G>T XP_016881276.1:n.2605-151G>T
NM_000271.5:c.2605-151G>T MANE Select NP_000262.2:n.2605-151G>T