Canonical Allele Identifier: CA2625667067

Gene: NPC2

Linked Data

• ClinVar Variation Id: 2984631
• ClinVar RCV Id: RCV003845774
• gnomAD v4: 14-74493177-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74493177C>T , CM000676.2:g.74493177C>T	GRCh38
NC_000014.8:g.74959880C>T , CM000676.1:g.74959880C>T	GRCh37
NC_000014.7:g.74029633C>T	NCBI36
NG_007117.1:g.5205G>A
NG_033074.1:g.4458C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000555619.6:c.82+16G>A MANE Select	ENSP00000451112.2:n.82+16G>A
ENST00000238633.6:c.82+16G>A	ENSP00000238633.2:n.82+16G>A
ENST00000434013.6:c.82+16G>A	ENSP00000412103.2:n.82+16G>A
ENST00000541064.5:c.82+16G>A	ENSP00000442488.1:n.82+16G>A
ENST00000553490.5:c.82+16G>A	ENSP00000451180.1:n.82+16G>A
ENST00000554482.1:c.50+16G>A	ENSP00000451314.1:n.50+16G>A
ENST00000555592.1:c.82+16G>A	ENSP00000450887.1:n.82+16G>A
ENST00000555619.5:c.82+16G>A	ENSP00000451112.1:n.82+16G>A
ENST00000556009.5:c.147+854G>A
ENST00000557510.5:c.82+16G>A	ENSP00000451206.1:n.82+16G>A
NM_006432.3:c.82+16G>A	NP_006423.1:n.82+16G>A
NM_001363688.1:c.82+16G>A	NP_001350617.1:n.82+16G>A
NM_006432.4:c.82+16G>A	NP_006423.1:n.82+16G>A
NM_001375440.1:c.82+16G>A	NP_001362369.1:n.82+16G>A
NM_006432.5:c.82+16G>A MANE Select	NP_006423.1:n.82+16G>A