Canonical Allele Identifier: CA2576470536
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23539486_23539487del , CM000680.2:g.23539486_23539487del GRCh38
NC_000018.9:g.21119450_21119451del , CM000680.1:g.21119450_21119451del GRCh37
NC_000018.8:g.19373448_19373449del NCBI36
NG_012795.1:g.52131_52132del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.2796-17_2796-16del MANE Select ENSP00000269228.4:n.2796-17_2796-16del
ENST00000269228.9:c.2796-17_2796-16del ENSP00000269228.4:n.2796-17_2796-16del
ENST00000591051.1:c.1874-17_1874-16del
ENST00000591075.1:n.412_413del
NM_000271.4:c.2796-17_2796-16del NP_000262.2:n.2796-17_2796-16del
XM_005258277.1:c.2847-17_2847-16del XP_005258334.1:n.2847-17_2847-16del
XM_005258278.3:c.2847-17_2847-16del XP_005258335.1:n.2847-17_2847-16del
XM_005258279.1:c.2796-17_2796-16del XP_005258336.1:n.2796-17_2796-16del
XM_006722479.2:c.2847-17_2847-16del XP_006722542.1:n.2847-17_2847-16del
XM_011526015.1:c.2382-17_2382-16del XP_011524317.1:n.2382-17_2382-16del
XM_005258278.5:c.2847-17_2847-16del XP_005258335.1:n.2847-17_2847-16del
XM_005258279.2:c.2796-17_2796-16del XP_005258336.1:n.2796-17_2796-16del
XM_006722479.3:c.2847-17_2847-16del XP_006722542.1:n.2847-17_2847-16del
XM_017025784.1:c.2847-17_2847-16del XP_016881273.1:n.2847-17_2847-16del
XM_017025785.1:c.2847-17_2847-16del XP_016881274.1:n.2847-17_2847-16del
XM_017025786.1:c.2796-17_2796-16del XP_016881275.1:n.2796-17_2796-16del
XM_017025787.1:c.2796-17_2796-16del XP_016881276.1:n.2796-17_2796-16del
NM_000271.5:c.2796-17_2796-16del MANE Select NP_000262.2:n.2796-17_2796-16del