Canonical Allele Identifier: CA2147069901

Gene: NPC2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74493167G= , CM000676.2:g.74493167G=	GRCh38
NC_000014.8:g.74959870G= , CM000676.1:g.74959870G=	GRCh37
NC_000014.7:g.74029623G=	NCBI36
NG_007117.1:g.5215C=
NG_033074.1:g.4448G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000555619.6:c.82+26C= MANE Select	ENSP00000451112.2:n.82+26C=
ENST00000238633.6:c.82+26C=	ENSP00000238633.2:n.82+26C=
ENST00000434013.6:c.82+26C=	ENSP00000412103.2:n.82+26C=
ENST00000541064.5:c.82+26C=	ENSP00000442488.1:n.82+26C=
ENST00000553490.5:c.82+26C=	ENSP00000451180.1:n.82+26C=
ENST00000554482.1:c.50+26C=	ENSP00000451314.1:n.50+26C=
ENST00000555592.1:c.82+26C=	ENSP00000450887.1:n.82+26C=
ENST00000555619.5:c.82+26C=	ENSP00000451112.1:n.82+26C=
ENST00000556009.5:c.147+864C=
ENST00000557510.5:c.82+26C=	ENSP00000451206.1:n.82+26C=
NM_006432.3:c.82+26C=	NP_006423.1:n.82+26C=
NM_001363688.1:c.82+26C=	NP_001350617.1:n.82+26C=
NM_006432.4:c.82+26C=	NP_006423.1:n.82+26C=
NM_001375440.1:c.82+26C=	NP_001362369.1:n.82+26C=
NM_006432.5:c.82+26C= MANE Select	NP_006423.1:n.82+26C=