Canonical Allele Identifier: CA487218812

Gene: NPC2

Linked Data

• MyVariant Identifiers: chr14:g.74951178G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74484475G>T , CM000676.2:g.74484475G>T	GRCh38
NC_000014.8:g.74951178G>T , CM000676.1:g.74951178G>T	GRCh37
NC_000014.7:g.74020931G>T	NCBI36
NG_007117.1:g.13907C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555619.6:c.303C>A MANE Select	ENSP00000451112.2:p.Ile101=
ENST00000238633.6:c.303C>A	ENSP00000238633.2:p.Ile101=
ENST00000434013.6:c.303C>A	ENSP00000412103.2:p.Ile101=
ENST00000541064.5:c.303C>A	ENSP00000442488.1:p.Ile101=
ENST00000553490.5:c.303C>A	ENSP00000451180.1:p.Ile101=
ENST00000554482.1:c.158+1854C>A	ENSP00000451314.1:n.158+1854C>A
ENST00000555592.1:c.303C>A	ENSP00000450887.1:p.Ile101=
ENST00000555619.5:c.303C>A	ENSP00000451112.1:p.Ile101=
ENST00000556009.5:c.368C>A
ENST00000557510.5:c.303C>A	ENSP00000451206.1:p.Ile101=
NM_006432.3:c.303C>A	NP_006423.1:p.Ile101=
NM_001363688.1:c.303C>A	NP_001350617.1:p.Ile101=
NM_006432.4:c.303C>A	NP_006423.1:p.Ile101=
NM_001375440.1:c.303C>A	NP_001362369.1:p.Ile101=
NM_006432.5:c.303C>A MANE Select	NP_006423.1:p.Ile101=