Canonical Allele Identifier: CA2641273908
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23540019_23540021del , CM000680.2:g.23540019_23540021del GRCh38
NC_000018.9:g.21119983_21119985del , CM000680.1:g.21119983_21119985del GRCh37
NC_000018.8:g.19373981_19373983del NCBI36
NG_012795.1:g.51599_51601del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269228.10:c.2605-18_2605-16del MANE Select ENSP00000269228.4:n.2605-18_2605-16del
ENST00000269228.9:c.2605-18_2605-16del ENSP00000269228.4:n.2605-18_2605-16del
ENST00000540608.5:n.2519-18_2519-16del
ENST00000586718.1:n.396-18_396-16del
ENST00000591051.1:c.1683-18_1683-16del
NM_000271.4:c.2605-18_2605-16del NP_000262.2:n.2605-18_2605-16del
XM_005258277.1:c.2656-18_2656-16del XP_005258334.1:n.2656-18_2656-16del
XM_005258278.3:c.2656-18_2656-16del XP_005258335.1:n.2656-18_2656-16del
XM_005258279.1:c.2605-18_2605-16del XP_005258336.1:n.2605-18_2605-16del
XM_006722479.2:c.2656-18_2656-16del XP_006722542.1:n.2656-18_2656-16del
XM_011526015.1:c.2191-18_2191-16del XP_011524317.1:n.2191-18_2191-16del
XM_005258278.5:c.2656-18_2656-16del XP_005258335.1:n.2656-18_2656-16del
XM_005258279.2:c.2605-18_2605-16del XP_005258336.1:n.2605-18_2605-16del
XM_006722479.3:c.2656-18_2656-16del XP_006722542.1:n.2656-18_2656-16del
XM_017025784.1:c.2656-18_2656-16del XP_016881273.1:n.2656-18_2656-16del
XM_017025785.1:c.2656-18_2656-16del XP_016881274.1:n.2656-18_2656-16del
XM_017025786.1:c.2605-18_2605-16del XP_016881275.1:n.2605-18_2605-16del
XM_017025787.1:c.2605-18_2605-16del XP_016881276.1:n.2605-18_2605-16del
NM_000271.5:c.2605-18_2605-16del MANE Select NP_000262.2:n.2605-18_2605-16del