Canonical Allele Identifier: CA297081332

Gene: NPC1

Linked Data

• dbSNP Id: rs1053188476
• gnomAD v2: 18-21119748-T-C
• gnomAD v3: 18-23539784-T-C
• gnomAD v4: 18-23539784-T-C
• MyVariant Identifiers: chr18:g.21119748T>C (hg19) ; chr18:g.23539784T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23539784T>C , CM000680.2:g.23539784T>C	GRCh38
NC_000018.9:g.21119748T>C , CM000680.1:g.21119748T>C	GRCh37
NC_000018.8:g.19373746T>C	NCBI36
NG_012795.1:g.51834A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.2795+27A>G MANE Select	ENSP00000269228.4:n.2795+27A>G
ENST00000269228.9:c.2795+27A>G	ENSP00000269228.4:n.2795+27A>G
ENST00000540608.5:n.2736A>G
ENST00000591051.1:c.1873+27A>G
ENST00000591075.1:n.115A>G
NM_000271.4:c.2795+27A>G	NP_000262.2:n.2795+27A>G
XM_005258277.1:c.2846+27A>G	XP_005258334.1:n.2846+27A>G
XM_005258278.3:c.2846+27A>G	XP_005258335.1:n.2846+27A>G
XM_005258279.1:c.2795+27A>G	XP_005258336.1:n.2795+27A>G
XM_006722479.2:c.2846+27A>G	XP_006722542.1:n.2846+27A>G
XM_011526015.1:c.2381+27A>G	XP_011524317.1:n.2381+27A>G
XM_005258278.5:c.2846+27A>G	XP_005258335.1:n.2846+27A>G
XM_005258279.2:c.2795+27A>G	XP_005258336.1:n.2795+27A>G
XM_006722479.3:c.2846+27A>G	XP_006722542.1:n.2846+27A>G
XM_017025784.1:c.2846+27A>G	XP_016881273.1:n.2846+27A>G
XM_017025785.1:c.2846+27A>G	XP_016881274.1:n.2846+27A>G
XM_017025786.1:c.2795+27A>G	XP_016881275.1:n.2795+27A>G
XM_017025787.1:c.2795+27A>G	XP_016881276.1:n.2795+27A>G
NM_000271.5:c.2795+27A>G MANE Select	NP_000262.2:n.2795+27A>G