Canonical Allele Identifier: CA390531267

Gene: NPC2

Linked Data

• MyVariant Identifiers: chr14:g.74947370T>G (hg19) ; chr14:g.74480667T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74480667T>G , CM000676.2:g.74480667T>G	GRCh38
NC_000014.8:g.74947370T>G , CM000676.1:g.74947370T>G	GRCh37
NC_000014.7:g.74017123T>G	NCBI36
NG_007117.1:g.17715A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555619.6:c.441+35A>C MANE Select	ENSP00000451112.2:n.441+35A>C
ENST00000238633.6:c.432+44A>C	ENSP00000238633.2:n.432+44A>C
ENST00000434013.6:c.441+35A>C	ENSP00000412103.2:n.441+35A>C
ENST00000541064.5:c.364-379A>C	ENSP00000442488.1:n.364-379A>C
ENST00000553490.5:c.457+19A>C	ENSP00000451180.1:n.457+19A>C
ENST00000554482.1:c.236+35A>C	ENSP00000451314.1:n.236+35A>C
ENST00000555619.5:c.441+35A>C	ENSP00000451112.1:n.441+35A>C
ENST00000556009.5:c.506+35A>C
ENST00000557510.5:c.476A>C	ENSP00000451206.1:p.Glu159Ala
NM_006432.3:c.441+35A>C	NP_006423.1:n.441+35A>C
NM_001363688.1:c.476A>C	NP_001350617.1:p.Glu159Ala
NM_006432.4:c.441+35A>C	NP_006423.1:n.441+35A>C
NM_001375440.1:c.364-379A>C	NP_001362369.1:n.364-379A>C
NM_006432.5:c.441+35A>C MANE Select	NP_006423.1:n.441+35A>C