Canonical Allele Identifier: CA1883798857

Gene: GLT6D1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135637821_135637822delinsAG , CM000671.2:g.135637821_135637822delinsAG	GRCh38
NC_000009.11:g.138529667_138529668delinsAG , CM000671.1:g.138529667_138529668delinsAG	GRCh37
NC_000009.10:g.137669488_137669489delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371763.6:c.71+1295_71+1296delinsCT MANE Select	ENSP00000360829.1:n.71+1295_71+1296delinsCT
ENST00000371763.5:c.71+1295_71+1296delinsCT	ENSP00000360829.1:n.71+1295_71+1296delinsCT
ENST00000613244.1:c.71+1295_71+1296delinsCT	ENSP00000483037.1:n.71+1295_71+1296delinsCT
NM_182974.2:c.71+1295_71+1296delinsCT	NP_892019.2:n.71+1295_71+1296delinsCT
XM_011518633.1:c.71+1295_71+1296delinsCT	XP_011516935.1:n.71+1295_71+1296delinsCT
XM_011518634.1:c.71+1295_71+1296delinsCT	XP_011516936.1:n.71+1295_71+1296delinsCT
XM_011518635.1:c.71+1295_71+1296delinsCT	XP_011516937.1:n.71+1295_71+1296delinsCT
XM_011518636.1:c.71+1295_71+1296delinsCT	XP_011516938.1:n.71+1295_71+1296delinsCT
XM_011518637.1:c.71+1295_71+1296delinsCT	XP_011516939.1:n.71+1295_71+1296delinsCT
XM_011518633.2:c.71+1295_71+1296delinsCT	XP_011516935.1:n.71+1295_71+1296delinsCT
XM_011518634.2:c.71+1295_71+1296delinsCT	XP_011516936.1:n.71+1295_71+1296delinsCT
XM_011518635.2:c.71+1295_71+1296delinsCT	XP_011516937.1:n.71+1295_71+1296delinsCT
XM_011518636.2:c.71+1295_71+1296delinsCT	XP_011516938.1:n.71+1295_71+1296delinsCT
XM_011518637.2:c.71+1295_71+1296delinsCT	XP_011516939.1:n.71+1295_71+1296delinsCT
XM_024447534.1:c.71+1295_71+1296delinsCT	XP_024303302.1:n.71+1295_71+1296delinsCT
NM_182974.3:c.71+1295_71+1296delinsCT MANE Select	NP_892019.2:n.71+1295_71+1296delinsCT