Canonical Allele Identifier: CA2756266622

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293325dup , CM000665.2:g.52293325dup	GRCh38
NC_000003.11:g.52327341dup , CM000665.1:g.52327341dup	GRCh37
NC_000003.10:g.52302381dup	NCBI36
NG_023246.1:g.10506dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*199dup MANE Select	ENSP00000389175.2:n.*199dup
ENST00000436784.6:c.*199dup	ENSP00000389175.2:n.*199dup
ENST00000471180.5:c.*77dup	ENSP00000417526.1:n.*77dup
ENST00000473032.5:c.*77dup	ENSP00000418951.1:n.*77dup
ENST00000486393.5:c.*1134dup	ENSP00000419868.1:n.*1134dup
ENST00000489173.1:n.1933dup
NM_145262.3:c.*199dup	NP_660305.2:n.*199dup
NR_026699.1:n.1869dup
NR_026700.1:n.861dup
NR_026701.1:n.1753dup
NR_026702.1:n.791dup
XM_005264878.2:c.*890dup	XP_005264935.1:n.*890dup
XR_245095.2:n.2908dup
XM_017005730.1:c.*199dup	XP_016861219.1:n.*199dup
XM_024453351.1:c.*199dup	XP_024309119.1:n.*199dup
XM_024453352.1:c.*890dup	XP_024309120.1:n.*890dup
XR_001740022.2:n.3559dup
XR_001740023.2:n.3083dup
XR_245095.4:n.2909dup
NM_145262.4:c.*199dup MANE Select	NP_660305.2:n.*199dup
NR_026699.2:n.1861dup
NR_026700.2:n.853dup
NR_026701.2:n.1745dup
NR_026702.2:n.783dup
NM_001144951.2:c.*890dup	NP_001138423.1:n.*890dup