Canonical Allele Identifier: CA74794450

Gene: GLT8D1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52700579del , CM000665.2:g.52700579del	GRCh38
NC_000003.11:g.52734595del , CM000665.1:g.52734595del	GRCh37
NC_000003.10:g.52709635del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018446.4:c.-36-69del MANE Select	NP_060916.1:n.-36-69del
ENST00000266014.11:c.-36-69del MANE Select	ENSP00000266014.5:n.-36-69del
NM_001010983.2:c.-36-69del	NP_001010983.1:n.-36-69del
NM_001010983.3:c.-36-69del	NP_001010983.1:n.-36-69del
NM_001278280.1:c.-36-69del	NP_001265209.1:n.-36-69del
NM_001278280.2:c.-36-69del	NP_001265209.1:n.-36-69del
NM_001278281.1:c.-36-69del	NP_001265210.1:n.-36-69del
NM_001278281.2:c.-36-69del	NP_001265210.1:n.-36-69del
NM_018446.3:c.-36-69del	NP_060916.1:n.-36-69del
NM_152932.2:c.-36-69del	NP_690909.1:n.-36-69del
NM_152932.3:c.-36-69del	NP_690909.1:n.-36-69del
ENST00000266014.9:c.-36-69del	ENSP00000266014.5:n.-36-69del
ENST00000394783.7:c.-36-69del	ENSP00000378263.3:n.-36-69del
ENST00000407584.7:c.-543-69del	ENSP00000385730.4:n.-543-69del
ENST00000464705.1:c.-36-69del	ENSP00000417858.1:n.-36-69del
ENST00000478968.6:c.-36-69del	ENSP00000419612.2:n.-36-69del
ENST00000479553.5:c.-105del	ENSP00000417713.1:n.-105del
ENST00000484163.5:n.237-69del
ENST00000487642.5:c.-36-69del	ENSP00000420462.1:n.-36-69del
ENST00000489119.5:c.-36-69del	ENSP00000417551.2:n.-36-69del
ENST00000491606.5:c.-36-69del	ENSP00000418853.1:n.-36-69del
ENST00000497436.5:c.-36-69del	ENSP00000420286.1:n.-36-69del
ENST00000497953.5:c.-36-69del	ENSP00000419094.1:n.-36-69del
XM_024453641.1:c.-36-69del	XP_024309409.1:n.-36-69del
XR_002959551.1:n.549-69del