Canonical Allele Identifier: CA1703813791

Gene: NPC1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44541278T= , CM000669.2:g.44541278T=	GRCh38
NC_000007.13:g.44580877T= , CM000669.1:g.44580877T=	GRCh37
NC_000007.12:g.44547402T=	NCBI36
NG_013088.1:g.5038A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381160.8:c.-19A= MANE Select	ENSP00000370552.3:n.-19A=
ENST00000289547.8:c.-19A=	ENSP00000289547.4:n.-19A=
ENST00000381160.7:c.-19A=	ENSP00000370552.3:n.-19A=
ENST00000423141.1:c.-19A=	ENSP00000404670.1:n.-19A=
ENST00000546276.5:c.-19A=	ENSP00000438033.1:n.-19A=
NM_001101648.1:c.-19A=	NP_001095118.1:n.-19A=
NM_001300967.1:c.-19A=	NP_001287896.1:n.-19A=
NM_013389.2:c.-19A=	NP_037521.2:n.-19A=
XM_011515326.1:c.-19A=	XP_011513628.1:n.-19A=
XM_011515327.1:c.-19A=	XP_011513629.1:n.-19A=
XM_011515326.3:c.-19A=	XP_011513628.1:n.-19A=
XR_002956423.1:n.374A=
NM_001101648.2:c.-19A= MANE Select	NP_001095118.1:n.-19A=
NM_001300967.2:c.-19A=	NP_001287896.1:n.-19A=
NM_013389.3:c.-19A=	NP_037521.2:n.-19A=