Canonical Allele Identifier: CA2290173041
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23554710G= , CM000680.2:g.23554710G= GRCh38
NC_000018.9:g.21134674G= , CM000680.1:g.21134674G= GRCh37
NC_000018.8:g.19388672G= NCBI36
NG_012795.1:g.36908C=

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.1553+48C= MANE Select ENSP00000269228.4:n.1553+48C=
ENST00000269228.9:c.1553+48C= ENSP00000269228.4:n.1553+48C=
ENST00000540608.5:n.1467+48C=
ENST00000590301.1:n.228+48C=
ENST00000591051.1:c.835+48C=
NM_000271.4:c.1553+48C= NP_000262.2:n.1553+48C=
XM_005258277.1:c.1604+48C= XP_005258334.1:n.1604+48C=
XM_005258278.3:c.1604+48C= XP_005258335.1:n.1604+48C=
XM_005258279.1:c.1553+48C= XP_005258336.1:n.1553+48C=
XM_006722479.2:c.1604+48C= XP_006722542.1:n.1604+48C=
XM_011526015.1:c.1139+48C= XP_011524317.1:n.1139+48C=
XM_005258278.5:c.1604+48C= XP_005258335.1:n.1604+48C=
XM_005258279.2:c.1553+48C= XP_005258336.1:n.1553+48C=
XM_006722479.3:c.1604+48C= XP_006722542.1:n.1604+48C=
XM_017025784.1:c.1604+48C= XP_016881273.1:n.1604+48C=
XM_017025785.1:c.1604+48C= XP_016881274.1:n.1604+48C=
XM_017025786.1:c.1553+48C= XP_016881275.1:n.1553+48C=
XM_017025787.1:c.1553+48C= XP_016881276.1:n.1553+48C=
NM_000271.5:c.1553+48C= MANE Select NP_000262.2:n.1553+48C=