Canonical Allele Identifier: CA860992676

Gene: GLT6D1

Linked Data

• dbSNP Id: rs1168311274
• gnomAD v3: 9-135637900-T-TA
• gnomAD v4: 9-135637900-T-TA
• MyVariant Identifiers: chr9:g.138529746_138529747insA (hg19) ; chr9:g.135637900_135637901insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135637901dup , CM000671.2:g.135637901dup	GRCh38
NC_000009.11:g.138529747dup , CM000671.1:g.138529747dup	GRCh37
NC_000009.10:g.137669568dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371763.6:c.71+1216dup MANE Select	ENSP00000360829.1:n.71+1216dup
ENST00000371763.5:c.71+1216dup	ENSP00000360829.1:n.71+1216dup
ENST00000613244.1:c.71+1216dup	ENSP00000483037.1:n.71+1216dup
NM_182974.2:c.71+1216dup	NP_892019.2:n.71+1216dup
XM_011518633.1:c.71+1216dup	XP_011516935.1:n.71+1216dup
XM_011518634.1:c.71+1216dup	XP_011516936.1:n.71+1216dup
XM_011518635.1:c.71+1216dup	XP_011516937.1:n.71+1216dup
XM_011518636.1:c.71+1216dup	XP_011516938.1:n.71+1216dup
XM_011518637.1:c.71+1216dup	XP_011516939.1:n.71+1216dup
XM_011518633.2:c.71+1216dup	XP_011516935.1:n.71+1216dup
XM_011518634.2:c.71+1216dup	XP_011516936.1:n.71+1216dup
XM_011518635.2:c.71+1216dup	XP_011516937.1:n.71+1216dup
XM_011518636.2:c.71+1216dup	XP_011516938.1:n.71+1216dup
XM_011518637.2:c.71+1216dup	XP_011516939.1:n.71+1216dup
XM_024447534.1:c.71+1216dup	XP_024303302.1:n.71+1216dup
NM_182974.3:c.71+1216dup MANE Select	NP_892019.2:n.71+1216dup