Canonical Allele Identifier: CA2641272448

Gene: NPC1

Linked Data

• gnomAD v4: 18-23551729-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23551730dup , CM000680.2:g.23551730dup	GRCh38
NC_000018.9:g.21131694dup , CM000680.1:g.21131694dup	GRCh37
NC_000018.8:g.19385692dup	NCBI36
NG_012795.1:g.39888dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.1554-3dup MANE Select	ENSP00000269228.4:n.1554-3dup
ENST00000269228.9:c.1554-3dup	ENSP00000269228.4:n.1554-3dup
ENST00000540608.5:n.1468-3dup
ENST00000590301.1:n.229-3dup
ENST00000591051.1:c.835+3028dup
NM_000271.4:c.1554-3dup	NP_000262.2:n.1554-3dup
XM_005258277.1:c.1605-3dup	XP_005258334.1:n.1605-3dup
XM_005258278.3:c.1605-3dup	XP_005258335.1:n.1605-3dup
XM_005258279.1:c.1554-3dup	XP_005258336.1:n.1554-3dup
XM_006722479.2:c.1605-3dup	XP_006722542.1:n.1605-3dup
XM_011526015.1:c.1140-3dup	XP_011524317.1:n.1140-3dup
XM_005258278.5:c.1605-3dup	XP_005258335.1:n.1605-3dup
XM_005258279.2:c.1554-3dup	XP_005258336.1:n.1554-3dup
XM_006722479.3:c.1605-3dup	XP_006722542.1:n.1605-3dup
XM_017025784.1:c.1605-3dup	XP_016881273.1:n.1605-3dup
XM_017025785.1:c.1605-3dup	XP_016881274.1:n.1605-3dup
XM_017025786.1:c.1554-3dup	XP_016881275.1:n.1554-3dup
XM_017025787.1:c.1554-3dup	XP_016881276.1:n.1554-3dup
NM_000271.5:c.1554-3dup MANE Select	NP_000262.2:n.1554-3dup