Canonical Allele Identifier: CA2641272485

Gene: NPC1

Linked Data

• gnomAD v4: 18-23551752-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23551755del , CM000680.2:g.23551755del	GRCh38
NC_000018.9:g.21131719del , CM000680.1:g.21131719del	GRCh37
NC_000018.8:g.19385717del	NCBI36
NG_012795.1:g.39865del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.1554-26del MANE Select	ENSP00000269228.4:n.1554-26del
ENST00000269228.9:c.1554-26del	ENSP00000269228.4:n.1554-26del
ENST00000540608.5:n.1468-26del
ENST00000590301.1:n.229-26del
ENST00000591051.1:c.835+3005del
NM_000271.4:c.1554-26del	NP_000262.2:n.1554-26del
XM_005258277.1:c.1605-26del	XP_005258334.1:n.1605-26del
XM_005258278.3:c.1605-26del	XP_005258335.1:n.1605-26del
XM_005258279.1:c.1554-26del	XP_005258336.1:n.1554-26del
XM_006722479.2:c.1605-26del	XP_006722542.1:n.1605-26del
XM_011526015.1:c.1140-26del	XP_011524317.1:n.1140-26del
XM_005258278.5:c.1605-26del	XP_005258335.1:n.1605-26del
XM_005258279.2:c.1554-26del	XP_005258336.1:n.1554-26del
XM_006722479.3:c.1605-26del	XP_006722542.1:n.1605-26del
XM_017025784.1:c.1605-26del	XP_016881273.1:n.1605-26del
XM_017025785.1:c.1605-26del	XP_016881274.1:n.1605-26del
XM_017025786.1:c.1554-26del	XP_016881275.1:n.1554-26del
XM_017025787.1:c.1554-26del	XP_016881276.1:n.1554-26del
NM_000271.5:c.1554-26del MANE Select	NP_000262.2:n.1554-26del