Canonical Allele Identifier: CA2641278132
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23544952_23544953insCCCCCCCCCCCCCCCCCACCCCCCCCCCC , CM000680.2:g.23544952_23544953insCCCCCCCCCCCCCCCCCACCCCCCCCCCC GRCh38
NC_000018.9:g.21124916_21124917insCCCCCCCCCCCCCCCCCACCCCCCCCCCC , CM000680.1:g.21124916_21124917insCCCCCCCCCCCCCCCCCACCCCCCCCCCC GRCh37
NC_000018.8:g.19378914_19378915insCCCCCCCCCCCCCCCCCACCCCCCCCCCC NCBI36
NG_012795.1:g.46674_46675insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000269228.4:n.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGG...
ENST00000269228.9:c.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000269228.4:n.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGG...
ENST00000540608.5:n.1861+16_1861+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000591051.1:c.1025+16_1025+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG
NM_000271.4:c.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG NP_000262.2:n.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_005258277.1:c.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005258334.1:n.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_005258278.3:c.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005258335.1:n.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_005258279.1:c.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005258336.1:n.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_006722479.2:c.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_006722542.1:n.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_011526015.1:c.1533+16_1533+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_011524317.1:n.1533+16_1533+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_005258278.5:c.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005258335.1:n.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_005258279.2:c.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_005258336.1:n.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_006722479.3:c.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_006722542.1:n.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_017025784.1:c.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_016881273.1:n.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_017025785.1:c.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_016881274.1:n.1998+16_1998+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_017025786.1:c.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_016881275.1:n.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
XM_017025787.1:c.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG XP_016881276.1:n.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGG...
NM_000271.5:c.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_000262.2:n.1947+16_1947+17insGGTGGGGGGGGGGGGGGGGGGGGGGGGGG...