Canonical Allele Identifier: CA2641271867

Gene: NPC1

Linked Data

• gnomAD v4: 18-23560281-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23560282del , CM000680.2:g.23560282del	GRCh38
NC_000018.9:g.21140246del , CM000680.1:g.21140246del	GRCh37
NC_000018.8:g.19394244del	NCBI36
NG_012795.1:g.31336del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.830del MANE Select	ENSP00000269228.4:p.Met277ArgfsTer?
ENST00000269228.9:c.830del	ENSP00000269228.4:p.Met277ArgfsTer?
ENST00000540608.5:n.744del
ENST00000591051.1:c.61del
NM_000271.4:c.830del	NP_000262.2:p.Met277ArgfsTer?
XM_005258277.1:c.830del	XP_005258334.1:p.Met277ArgfsTer?
XM_005258278.3:c.830del	XP_005258335.1:p.Met277ArgfsTer?
XM_005258279.1:c.830del	XP_005258336.1:p.Met277ArgfsTer?
XM_006722479.2:c.830del	XP_006722542.1:p.Met277ArgfsTer?
XM_011526015.1:c.365del	XP_011524317.1:p.Met122ArgfsTer?
XM_005258278.5:c.830del	XP_005258335.1:p.Met277ArgfsTer?
XM_005258279.2:c.830del	XP_005258336.1:p.Met277ArgfsTer?
XM_006722479.3:c.830del	XP_006722542.1:p.Met277ArgfsTer?
XM_017025784.1:c.830del	XP_016881273.1:p.Met277ArgfsTer?
XM_017025785.1:c.830del	XP_016881274.1:p.Met277ArgfsTer?
XM_017025786.1:c.830del	XP_016881275.1:p.Met277ArgfsTer?
XM_017025787.1:c.830del	XP_016881276.1:p.Met277ArgfsTer?
NM_000271.5:c.830del MANE Select	NP_000262.2:p.Met277ArgfsTer?