Canonical Allele Identifier: CA1703813806
Gene: NPC1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44541283G= , CM000669.2:g.44541283G= GRCh38
NC_000007.13:g.44580882G= , CM000669.1:g.44580882G= GRCh37
NC_000007.12:g.44547407G= NCBI36
NG_013088.1:g.5033C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381160.8:c.-24C= MANE Select ENSP00000370552.3:n.-24C=
ENST00000289547.8:c.-24C= ENSP00000289547.4:n.-24C=
ENST00000381160.7:c.-24C= ENSP00000370552.3:n.-24C=
ENST00000423141.1:c.-24C= ENSP00000404670.1:n.-24C=
ENST00000546276.5:c.-24C= ENSP00000438033.1:n.-24C=
NM_001101648.1:c.-24C= NP_001095118.1:n.-24C=
NM_001300967.1:c.-24C= NP_001287896.1:n.-24C=
NM_013389.2:c.-24C= NP_037521.2:n.-24C=
XM_011515326.1:c.-24C= XP_011513628.1:n.-24C=
XM_011515327.1:c.-24C= XP_011513629.1:n.-24C=
XM_011515326.3:c.-24C= XP_011513628.1:n.-24C=
XR_002956423.1:n.369C=
NM_001101648.2:c.-24C= MANE Select NP_001095118.1:n.-24C=
NM_001300967.2:c.-24C= NP_001287896.1:n.-24C=
NM_013389.3:c.-24C= NP_037521.2:n.-24C=