Canonical Allele Identifier: CA2665985218

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293328-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293333dup , CM000665.2:g.52293333dup	GRCh38
NC_000003.11:g.52327349dup , CM000665.1:g.52327349dup	GRCh37
NC_000003.10:g.52302389dup	NCBI36
NG_023246.1:g.10514dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*207dup MANE Select	ENSP00000389175.2:n.*207dup
ENST00000436784.6:c.*207dup	ENSP00000389175.2:n.*207dup
ENST00000471180.5:c.*85dup	ENSP00000417526.1:n.*85dup
ENST00000473032.5:c.*85dup	ENSP00000418951.1:n.*85dup
ENST00000486393.5:c.*1142dup	ENSP00000419868.1:n.*1142dup
ENST00000489173.1:n.1941dup
NM_145262.3:c.*207dup	NP_660305.2:n.*207dup
NR_026699.1:n.1877dup
NR_026700.1:n.869dup
NR_026701.1:n.1761dup
NR_026702.1:n.799dup
XM_005264878.2:c.*898dup	XP_005264935.1:n.*898dup
XR_245095.2:n.2916dup
XM_017005730.1:c.*207dup	XP_016861219.1:n.*207dup
XM_024453351.1:c.*207dup	XP_024309119.1:n.*207dup
XM_024453352.1:c.*898dup	XP_024309120.1:n.*898dup
XR_001740022.2:n.3567dup
XR_001740023.2:n.3091dup
XR_245095.4:n.2917dup
NM_145262.4:c.*207dup MANE Select	NP_660305.2:n.*207dup
NR_026699.2:n.1869dup
NR_026700.2:n.861dup
NR_026701.2:n.1753dup
NR_026702.2:n.791dup
NM_001144951.2:c.*898dup	NP_001138423.1:n.*898dup