Canonical Allele Identifier: CA543056383

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1559467444
• gnomAD v2: 3-52327131-C-CG
• gnomAD v4: 3-52293115-C-CG
• MyVariant Identifiers: chr3:g.52327131_52327132insG (hg19) ; chr3:g.52293115_52293116insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293117dup , CM000665.2:g.52293117dup	GRCh38
NC_000003.11:g.52327133dup , CM000665.1:g.52327133dup	GRCh37
NC_000003.10:g.52302173dup	NCBI36
NG_023246.1:g.10298dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1563dup MANE Select	ENSP00000389175.2:p.Pro522AlafsTer6
ENST00000436784.6:c.1563dup	ENSP00000389175.2:p.Pro522AlafsTer6
ENST00000461183.5:c.835dup	ENSP00000417264.1:p.Ala279GlyfsTer?
ENST00000471180.5:c.706dup	ENSP00000417526.1:p.Ala236GlyfsTer?
ENST00000473032.5:c.601dup	ENSP00000418951.1:p.Ala201GlyfsTer?
ENST00000486393.5:c.*926dup	ENSP00000419868.1:n.*926dup
ENST00000489173.1:n.1857dup
NM_145262.3:c.1563dup	NP_660305.2:p.Pro522AlafsTer6
NR_026699.1:n.1661dup
NR_026700.1:n.767dup
NR_026701.1:n.1659dup
NR_026702.1:n.697dup
XM_005264878.2:c.*682dup	XP_005264935.1:n.*682dup
XR_245095.2:n.2814dup
XM_017005730.1:c.1182dup	XP_016861219.1:p.Pro395AlafsTer6
XM_024453351.1:c.1563dup	XP_024309119.1:p.Pro522AlafsTer6
XM_024453352.1:c.*682dup	XP_024309120.1:n.*682dup
XR_001740022.2:n.3465dup
XR_001740023.2:n.2989dup
XR_245095.4:n.2815dup
NM_145262.4:c.1563dup MANE Select	NP_660305.2:p.Pro522AlafsTer6
NR_026699.2:n.1653dup
NR_026700.2:n.759dup
NR_026701.2:n.1651dup
NR_026702.2:n.689dup
NM_001144951.2:c.*682dup	NP_001138423.1:n.*682dup