Canonical Allele Identifier: CA2641273212
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23539606_23539607dup , CM000680.2:g.23539606_23539607dup GRCh38
NC_000018.9:g.21119570_21119571dup , CM000680.1:g.21119570_21119571dup GRCh37
NC_000018.8:g.19373568_19373569dup NCBI36
NG_012795.1:g.52011_52012dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.2796-137_2796-136dup MANE Select ENSP00000269228.4:n.2796-137_2796-136dup
ENST00000269228.9:c.2796-137_2796-136dup ENSP00000269228.4:n.2796-137_2796-136dup
ENST00000591051.1:c.1874-137_1874-136dup
ENST00000591075.1:n.292_293dup
NM_000271.4:c.2796-137_2796-136dup NP_000262.2:n.2796-137_2796-136dup
XM_005258277.1:c.2847-137_2847-136dup XP_005258334.1:n.2847-137_2847-136dup
XM_005258278.3:c.2847-137_2847-136dup XP_005258335.1:n.2847-137_2847-136dup
XM_005258279.1:c.2796-137_2796-136dup XP_005258336.1:n.2796-137_2796-136dup
XM_006722479.2:c.2847-137_2847-136dup XP_006722542.1:n.2847-137_2847-136dup
XM_011526015.1:c.2382-137_2382-136dup XP_011524317.1:n.2382-137_2382-136dup
XM_005258278.5:c.2847-137_2847-136dup XP_005258335.1:n.2847-137_2847-136dup
XM_005258279.2:c.2796-137_2796-136dup XP_005258336.1:n.2796-137_2796-136dup
XM_006722479.3:c.2847-137_2847-136dup XP_006722542.1:n.2847-137_2847-136dup
XM_017025784.1:c.2847-137_2847-136dup XP_016881273.1:n.2847-137_2847-136dup
XM_017025785.1:c.2847-137_2847-136dup XP_016881274.1:n.2847-137_2847-136dup
XM_017025786.1:c.2796-137_2796-136dup XP_016881275.1:n.2796-137_2796-136dup
XM_017025787.1:c.2796-137_2796-136dup XP_016881276.1:n.2796-137_2796-136dup
NM_000271.5:c.2796-137_2796-136dup MANE Select NP_000262.2:n.2796-137_2796-136dup