Canonical Allele Identifier: CA2147066219
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74484421A= , CM000676.2:g.74484421A= GRCh38
NC_000014.8:g.74951124A= , CM000676.1:g.74951124A= GRCh37
NC_000014.7:g.74020877A= NCBI36
NG_007117.1:g.13961T=

Transcript Alleles

HGVS Amino-acid change
ENST00000555619.6:c.357T= MANE Select ENSP00000451112.2:p.Tyr119=
ENST00000238633.6:c.357T= ENSP00000238633.2:p.Tyr119=
ENST00000434013.6:c.357T= ENSP00000412103.2:p.Tyr119=
ENST00000541064.5:c.357T= ENSP00000442488.1:p.Tyr119=
ENST00000553490.5:c.357T= ENSP00000451180.1:p.Tyr119=
ENST00000554482.1:c.158+1908T= ENSP00000451314.1:n.158+1908T=
ENST00000555592.1:c.357T= ENSP00000450887.1:p.Tyr119=
ENST00000555619.5:c.357T= ENSP00000451112.1:p.Tyr119=
ENST00000556009.5:c.422T=
ENST00000557510.5:c.357T= ENSP00000451206.1:p.Tyr119=
NM_006432.3:c.357T= NP_006423.1:p.Tyr119=
NM_001363688.1:c.357T= NP_001350617.1:p.Tyr119=
NM_006432.4:c.357T= NP_006423.1:p.Tyr119=
NM_001375440.1:c.357T= NP_001362369.1:p.Tyr119=
NM_006432.5:c.357T= MANE Select NP_006423.1:p.Tyr119=