Canonical Allele Identifier: CA2147059449

Gene: NPC2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74480722A= , CM000676.2:g.74480722A=	GRCh38
NC_000014.8:g.74947425A= , CM000676.1:g.74947425A=	GRCh37
NC_000014.7:g.74017178A=	NCBI36
NG_007117.1:g.17660T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555619.6:c.421T= MANE Select	ENSP00000451112.2:p.Trp141=
ENST00000238633.6:c.421T=	ENSP00000238633.2:p.Trp141=
ENST00000434013.6:c.421T=	ENSP00000412103.2:p.Trp141=
ENST00000541064.5:c.364-434T=	ENSP00000442488.1:n.364-434T=
ENST00000553490.5:c.421T=	ENSP00000451180.1:p.Trp141=
ENST00000554482.1:c.216T=	ENSP00000451314.1:n.216T=
ENST00000555619.5:c.421T=	ENSP00000451112.1:p.Trp141=
ENST00000556009.5:c.486T=
ENST00000557510.5:c.421T=	ENSP00000451206.1:p.Trp141=
NM_006432.3:c.421T=	NP_006423.1:p.Trp141=
NM_001363688.1:c.421T=	NP_001350617.1:p.Trp141=
NM_006432.4:c.421T=	NP_006423.1:p.Trp141=
NM_001375440.1:c.364-434T=	NP_001362369.1:n.364-434T=
NM_006432.5:c.421T= MANE Select	NP_006423.1:p.Trp141=