Canonical Allele Identifier: CA1364976241

Gene: GNL3

Genomic Alleles

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

Transcript Alleles

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