Canonical Allele Identifier: CA542915337
Gene: GNL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52686064A>T , CM000665.2:g.52686064A>T GRCh38
NC_000003.11:g.52720080A>T , CM000665.1:g.52720080A>T GRCh37
NC_000003.10:g.52695120A>T NCBI36
NG_027871.1:g.5145A>T
NG_032108.1:g.4787T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000418458.6:c.-29A>T MANE Select ENSP00000395772.1:n.-29A>T
ENST00000394799.6:c.-162A>T ENSP00000378278.2:n.-162A>T
ENST00000418458.5:c.-29A>T ENSP00000395772.1:n.-29A>T
ENST00000462550.5:n.33A>T
ENST00000468146.5:n.60A>T
ENST00000468885.1:n.35A>T
ENST00000479230.5:c.-23-705A>T ENSP00000419734.1:n.-23-705A>T
ENST00000492349.5:c.-29A>T ENSP00000420345.1:n.-29A>T
ENST00000496254.5:n.16A>T
NM_014366.4:c.-29A>T NP_055181.3:n.-29A>T
NM_206825.1:c.-162A>T NP_996561.1:n.-162A>T
NM_206826.1:c.-24+9A>T NP_996562.1:n.-24+9A>T
NM_014366.5:c.-29A>T MANE Select NP_055181.3:n.-29A>T
NM_206825.2:c.-162A>T NP_996561.1:n.-162A>T