Canonical Allele Identifier: CA1364980992

Gene: GLT8D1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52699090C= , CM000665.2:g.52699090C=	GRCh38
NC_000003.11:g.52733106C= , CM000665.1:g.52733106C=	GRCh37
NC_000003.10:g.52708146C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018446.4:c.116-1156G= MANE Select	NP_060916.1:n.116-1156G=
ENST00000266014.11:c.116-1156G= MANE Select	ENSP00000266014.5:n.116-1156G=
NM_001010983.2:c.116-1156G=	NP_001010983.1:n.116-1156G=
NM_001010983.3:c.116-1156G=	NP_001010983.1:n.116-1156G=
NM_001278280.1:c.116-1156G=	NP_001265209.1:n.116-1156G=
NM_001278280.2:c.116-1156G=	NP_001265209.1:n.116-1156G=
NM_001278281.1:c.116-1156G=	NP_001265210.1:n.116-1156G=
NM_001278281.2:c.116-1156G=	NP_001265210.1:n.116-1156G=
NM_018446.3:c.116-1156G=	NP_060916.1:n.116-1156G=
NM_152932.2:c.116-1156G=	NP_690909.1:n.116-1156G=
NM_152932.3:c.116-1156G=	NP_690909.1:n.116-1156G=
ENST00000266014.9:c.116-1156G=	ENSP00000266014.5:n.116-1156G=
ENST00000394783.7:c.116-1156G=	ENSP00000378263.3:n.116-1156G=
ENST00000407584.7:c.-392-1156G=	ENSP00000385730.4:n.-392-1156G=
ENST00000478968.6:c.116-1156G=	ENSP00000419612.2:n.116-1156G=
ENST00000479553.5:c.116-1156G=	ENSP00000417713.1:n.116-1156G=
ENST00000484163.5:n.388-1156G=
ENST00000485899.1:n.153-1156G=
ENST00000487642.5:c.116-1156G=	ENSP00000420462.1:n.116-1156G=
ENST00000489119.5:c.116-1156G=	ENSP00000417551.2:n.116-1156G=
ENST00000491606.5:c.116-1156G=	ENSP00000418853.1:n.116-1156G=
ENST00000497436.5:c.116-1156G=	ENSP00000420286.1:n.116-1156G=
ENST00000497953.5:c.116-1156G=	ENSP00000419094.1:n.116-1156G=
XM_024453641.1:c.116-1156G=	XP_024309409.1:n.116-1156G=
XR_002959551.1:n.700-1156G=