Canonical Allele Identifier: CA2695227434

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23538540dup , CM000680.2:g.23538540dup	GRCh38
NC_000018.9:g.21118504dup , CM000680.1:g.21118504dup	GRCh37
NC_000018.8:g.19372502dup	NCBI36
NG_012795.1:g.53078dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269228.10:c.3041+2dup MANE Select	ENSP00000269228.4:n.3041+2dup
ENST00000269228.9:c.3041+2dup	ENSP00000269228.4:n.3041+2dup
ENST00000591051.1:c.2119+2dup
ENST00000591075.1:n.674+2dup
ENST00000591955.1:n.384+2dup
NM_000271.4:c.3041+2dup	NP_000262.2:n.3041+2dup
XM_005258277.1:c.3092+2dup	XP_005258334.1:n.3092+2dup
XM_005258278.3:c.3092+2dup	XP_005258335.1:n.3092+2dup
XM_005258279.1:c.3041+2dup	XP_005258336.1:n.3041+2dup
XM_006722479.2:c.3092+2dup	XP_006722542.1:n.3092+2dup
XM_011526015.1:c.2627+2dup	XP_011524317.1:n.2627+2dup
XM_005258278.5:c.3092+2dup	XP_005258335.1:n.3092+2dup
XM_005258279.2:c.3041+2dup	XP_005258336.1:n.3041+2dup
XM_006722479.3:c.3092+2dup	XP_006722542.1:n.3092+2dup
XM_017025784.1:c.3092+2dup	XP_016881273.1:n.3092+2dup
XM_017025785.1:c.3092+2dup	XP_016881274.1:n.3092+2dup
XM_017025786.1:c.3041+2dup	XP_016881275.1:n.3041+2dup
XM_017025787.1:c.3041+2dup	XP_016881276.1:n.3041+2dup
NM_000271.5:c.3041+2dup MANE Select	NP_000262.2:n.3041+2dup