Canonical Allele Identifier: CA2290165654
Gene: NPC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23539229T= , CM000680.2:g.23539229T= GRCh38
NC_000018.9:g.21119193T= , CM000680.1:g.21119193T= GRCh37
NC_000018.8:g.19373191T= NCBI36
NG_012795.1:g.52389A=

Transcript Alleles

HGVS Amino-acid change
ENST00000269228.10:c.2911+126A= MANE Select ENSP00000269228.4:n.2911+126A=
ENST00000269228.9:c.2911+126A= ENSP00000269228.4:n.2911+126A=
ENST00000591051.1:c.1989+126A=
ENST00000591075.1:n.544+126A=
NM_000271.4:c.2911+126A= NP_000262.2:n.2911+126A=
XM_005258277.1:c.2962+126A= XP_005258334.1:n.2962+126A=
XM_005258278.3:c.2962+126A= XP_005258335.1:n.2962+126A=
XM_005258279.1:c.2911+126A= XP_005258336.1:n.2911+126A=
XM_006722479.2:c.2962+126A= XP_006722542.1:n.2962+126A=
XM_011526015.1:c.2497+126A= XP_011524317.1:n.2497+126A=
XM_005258278.5:c.2962+126A= XP_005258335.1:n.2962+126A=
XM_005258279.2:c.2911+126A= XP_005258336.1:n.2911+126A=
XM_006722479.3:c.2962+126A= XP_006722542.1:n.2962+126A=
XM_017025784.1:c.2962+126A= XP_016881273.1:n.2962+126A=
XM_017025785.1:c.2962+126A= XP_016881274.1:n.2962+126A=
XM_017025786.1:c.2911+126A= XP_016881275.1:n.2911+126A=
XM_017025787.1:c.2911+126A= XP_016881276.1:n.2911+126A=
NM_000271.5:c.2911+126A= MANE Select NP_000262.2:n.2911+126A=