Canonical Allele Identifier: CA2641278119
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23544952_23544953insCCCCCCCCCCCCCCACCCCCCCCCCCCCC , CM000680.2:g.23544952_23544953insCCCCCCCCCCCCCCACCCCCCCCCCCCCC GRCh38
NC_000018.9:g.21124916_21124917insCCCCCCCCCCCCCCACCCCCCCCCCCCCC , CM000680.1:g.21124916_21124917insCCCCCCCCCCCCCCACCCCCCCCCCCCCC GRCh37
NC_000018.8:g.19378914_19378915insCCCCCCCCCCCCCCACCCCCCCCCCCCCC NCBI36
NG_012795.1:g.46674_46675insGGGGGTGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

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