Canonical Allele Identifier: CA401777212

Gene: NPC1

Linked Data

• ClinVar Variation Id: 1705794
• ClinVar RCV Id: RCV002284104
• gnomAD v4: 18-23556283-A-C
• MyVariant Identifiers: chr18:g.21136247A>C (hg19) ; chr18:g.23556283A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23556283A>C , CM000680.2:g.23556283A>C	GRCh38
NC_000018.9:g.21136247A>C , CM000680.1:g.21136247A>C	GRCh37
NC_000018.8:g.19390245A>C	NCBI36
NG_012795.1:g.35335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.1286T>G MANE Select	ENSP00000269228.4:p.Val429Gly
ENST00000269228.9:c.1286T>G	ENSP00000269228.4:p.Val429Gly
ENST00000540608.5:n.1200T>G
ENST00000591051.1:c.568T>G
NM_000271.4:c.1286T>G	NP_000262.2:p.Val429Gly
XM_005258277.1:c.1337T>G	XP_005258334.1:p.Val446Gly
XM_005258278.3:c.1337T>G	XP_005258335.1:p.Val446Gly
XM_005258279.1:c.1286T>G	XP_005258336.1:p.Val429Gly
XM_006722479.2:c.1337T>G	XP_006722542.1:p.Val446Gly
XM_011526015.1:c.872T>G	XP_011524317.1:p.Val291Gly
XM_005258278.5:c.1337T>G	XP_005258335.1:p.Val446Gly
XM_005258279.2:c.1286T>G	XP_005258336.1:p.Val429Gly
XM_006722479.3:c.1337T>G	XP_006722542.1:p.Val446Gly
XM_017025784.1:c.1337T>G	XP_016881273.1:p.Val446Gly
XM_017025785.1:c.1337T>G	XP_016881274.1:p.Val446Gly
XM_017025786.1:c.1286T>G	XP_016881275.1:p.Val429Gly
XM_017025787.1:c.1286T>G	XP_016881276.1:p.Val429Gly
NM_000271.5:c.1286T>G MANE Select	NP_000262.2:p.Val429Gly