Canonical Allele Identifier: CA2641276179
Gene: NPC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23532381_23532382del , CM000680.2:g.23532381_23532382del GRCh38
NC_000018.9:g.21112345_21112346del , CM000680.1:g.21112345_21112346del GRCh37
NC_000018.8:g.19366343_19366344del NCBI36
NG_012795.1:g.59236_59237del
NG_033119.1:g.33912_33913del

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.3755-98_3755-97del MANE Select ENSP00000269228.4:n.3755-98_3755-97del
ENST00000269228.9:c.3755-98_3755-97del ENSP00000269228.4:n.3755-98_3755-97del
ENST00000586150.5:c.509+973_509+974del
ENST00000588867.1:n.1438-98_1438-97del
ENST00000590723.5:c.163+973_163+974del ENSP00000464755.1:n.163+973_163+974del
ENST00000591051.1:c.2833-98_2833-97del
ENST00000591107.6:c.431+973_431+974del
ENST00000593280.2:c.86+973_86+974del
NM_000271.4:c.3755-98_3755-97del NP_000262.2:n.3755-98_3755-97del
XM_005258277.1:c.3805+973_3805+974del XP_005258334.1:n.3805+973_3805+974del
XM_005258278.3:c.3806-98_3806-97del XP_005258335.1:n.3806-98_3806-97del
XM_005258279.1:c.3754+973_3754+974del XP_005258336.1:n.3754+973_3754+974del
XM_006722479.2:c.3805+973_3805+974del XP_006722542.1:n.3805+973_3805+974del
XM_011526015.1:c.3340+973_3340+974del XP_011524317.1:n.3340+973_3340+974del
XM_005258278.5:c.3806-98_3806-97del XP_005258335.1:n.3806-98_3806-97del
XM_005258279.2:c.3754+973_3754+974del XP_005258336.1:n.3754+973_3754+974del
XM_006722479.3:c.3805+973_3805+974del XP_006722542.1:n.3805+973_3805+974del
XM_017025784.1:c.3805+973_3805+974del XP_016881273.1:n.3805+973_3805+974del
XM_017025785.1:c.3805+973_3805+974del XP_016881274.1:n.3805+973_3805+974del
XM_017025786.1:c.3754+973_3754+974del XP_016881275.1:n.3754+973_3754+974del
XM_017025787.1:c.3754+973_3754+974del XP_016881276.1:n.3754+973_3754+974del
NM_000271.5:c.3755-98_3755-97del MANE Select NP_000262.2:n.3755-98_3755-97del