Canonical Allele Identifier: CA2147059271

Gene: NPC2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74480633A= , CM000676.2:g.74480633A=	GRCh38
NC_000014.8:g.74947336A= , CM000676.1:g.74947336A=	GRCh37
NC_000014.7:g.74017089A=	NCBI36
NG_007117.1:g.17749T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555619.6:c.441+69T= MANE Select	ENSP00000451112.2:n.441+69T=
ENST00000238633.6:c.432+78T=	ENSP00000238633.2:n.432+78T=
ENST00000434013.6:c.441+69T=	ENSP00000412103.2:n.441+69T=
ENST00000541064.5:c.364-345T=	ENSP00000442488.1:n.364-345T=
ENST00000553490.5:c.457+53T=	ENSP00000451180.1:n.457+53T=
ENST00000554482.1:c.236+69T=	ENSP00000451314.1:n.236+69T=
ENST00000555619.5:c.441+69T=	ENSP00000451112.1:n.441+69T=
ENST00000556009.5:c.506+69T=
ENST00000557510.5:c.510T=	ENSP00000451206.1:p.Thr170=
NM_006432.3:c.441+69T=	NP_006423.1:n.441+69T=
NM_001363688.1:c.510T=	NP_001350617.1:p.Thr170=
NM_006432.4:c.441+69T=	NP_006423.1:n.441+69T=
NM_001375440.1:c.364-345T=	NP_001362369.1:n.364-345T=
NM_006432.5:c.441+69T= MANE Select	NP_006423.1:n.441+69T=