Canonical Allele Identifier: CA2147066286
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74484581T= , CM000676.2:g.74484581T= GRCh38
NC_000014.8:g.74951284T= , CM000676.1:g.74951284T= GRCh37
NC_000014.7:g.74021037T= NCBI36
NG_007117.1:g.13801A=

Transcript Alleles

HGVS Amino-acid change
ENST00000555619.6:c.197A= MANE Select ENSP00000451112.2:p.Gln66=
ENST00000238633.6:c.197A= ENSP00000238633.2:p.Gln66=
ENST00000434013.6:c.197A= ENSP00000412103.2:p.Gln66=
ENST00000541064.5:c.197A= ENSP00000442488.1:p.Gln66=
ENST00000553490.5:c.197A= ENSP00000451180.1:p.Gln66=
ENST00000554482.1:c.158+1748A= ENSP00000451314.1:n.158+1748A=
ENST00000555592.1:c.197A= ENSP00000450887.1:p.Gln66=
ENST00000555619.5:c.197A= ENSP00000451112.1:p.Gln66=
ENST00000556009.5:c.262A=
ENST00000557510.5:c.197A= ENSP00000451206.1:p.Gln66=
NM_006432.3:c.197A= NP_006423.1:p.Gln66=
NM_001363688.1:c.197A= NP_001350617.1:p.Gln66=
NM_006432.4:c.197A= NP_006423.1:p.Gln66=
NM_001375440.1:c.197A= NP_001362369.1:p.Gln66=
NM_006432.5:c.197A= MANE Select NP_006423.1:p.Gln66=