Canonical Allele Identifier: CA2665985136

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293212-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293213dup , CM000665.2:g.52293213dup	GRCh38
NC_000003.11:g.52327229dup , CM000665.1:g.52327229dup	GRCh37
NC_000003.10:g.52302269dup	NCBI36
NG_023246.1:g.10394dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*87dup MANE Select	ENSP00000389175.2:n.*87dup
ENST00000436784.6:c.*87dup	ENSP00000389175.2:n.*87dup
ENST00000471180.5:c.*58+21dup	ENSP00000417526.1:n.*58+21dup
ENST00000473032.5:c.*58+21dup	ENSP00000418951.1:n.*58+21dup
ENST00000486393.5:c.*1022dup	ENSP00000419868.1:n.*1022dup
ENST00000489173.1:n.1914+39dup
NM_145262.3:c.*87dup	NP_660305.2:n.*87dup
NR_026699.1:n.1757dup
NR_026700.1:n.842+21dup
NR_026701.1:n.1734+21dup
NR_026702.1:n.772+21dup
XM_005264878.2:c.*778dup	XP_005264935.1:n.*778dup
XR_245095.2:n.2889+21dup
XM_017005730.1:c.*87dup	XP_016861219.1:n.*87dup
XM_024453351.1:c.*87dup	XP_024309119.1:n.*87dup
XM_024453352.1:c.*778dup	XP_024309120.1:n.*778dup
XR_001740022.2:n.3540+21dup
XR_001740023.2:n.3064+21dup
XR_245095.4:n.2890+21dup
NM_145262.4:c.*87dup MANE Select	NP_660305.2:n.*87dup
NR_026699.2:n.1749dup
NR_026700.2:n.834+21dup
NR_026701.2:n.1726+21dup
NR_026702.2:n.764+21dup
NM_001144951.2:c.*778dup	NP_001138423.1:n.*778dup