Canonical Allele Identifier: CA487214012

Gene: NPC2

Linked Data

• MyVariant Identifiers: chr14:g.74947411T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74480708T>C , CM000676.2:g.74480708T>C	GRCh38
NC_000014.8:g.74947411T>C , CM000676.1:g.74947411T>C	GRCh37
NC_000014.7:g.74017164T>C	NCBI36
NG_007117.1:g.17674A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000555619.6:c.435A>G MANE Select	ENSP00000451112.2:p.Val145=
ENST00000238633.6:c.432+3A>G	ENSP00000238633.2:n.432+3A>G
ENST00000434013.6:c.435A>G	ENSP00000412103.2:p.Val145=
ENST00000541064.5:c.364-420A>G	ENSP00000442488.1:n.364-420A>G
ENST00000553490.5:c.435A>G	ENSP00000451180.1:p.Val145=
ENST00000554482.1:c.230A>G	ENSP00000451314.1:n.230A>G
ENST00000555619.5:c.435A>G	ENSP00000451112.1:p.Val145=
ENST00000556009.5:c.500A>G
ENST00000557510.5:c.435A>G	ENSP00000451206.1:p.Val145=
NM_006432.3:c.435A>G	NP_006423.1:p.Val145=
NM_001363688.1:c.435A>G	NP_001350617.1:p.Val145=
NM_006432.4:c.435A>G	NP_006423.1:p.Val145=
NM_001375440.1:c.364-420A>G	NP_001362369.1:n.364-420A>G
NM_006432.5:c.435A>G MANE Select	NP_006423.1:p.Val145=