Canonical Allele Identifier: CA2840119990

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293173dup , CM000665.2:g.52293173dup	GRCh38
NC_000003.11:g.52327189dup , CM000665.1:g.52327189dup	GRCh37
NC_000003.10:g.52302229dup	NCBI36
NG_023246.1:g.10354dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*47dup MANE Select	ENSP00000389175.2:n.*47dup
ENST00000436784.6:c.*47dup	ENSP00000389175.2:n.*47dup
ENST00000471180.5:c.*39dup	ENSP00000417526.1:n.*39dup
ENST00000473032.5:c.*39dup	ENSP00000418951.1:n.*39dup
ENST00000486393.5:c.*982dup	ENSP00000419868.1:n.*982dup
ENST00000489173.1:n.1913dup
NM_145262.3:c.*47dup	NP_660305.2:n.*47dup
NR_026699.1:n.1717dup
NR_026700.1:n.823dup
NR_026701.1:n.1715dup
NR_026702.1:n.753dup
XM_005264878.2:c.*738dup	XP_005264935.1:n.*738dup
XR_245095.2:n.2870dup
XM_017005730.1:c.*47dup	XP_016861219.1:n.*47dup
XM_024453351.1:c.*47dup	XP_024309119.1:n.*47dup
XM_024453352.1:c.*738dup	XP_024309120.1:n.*738dup
XR_001740022.2:n.3521dup
XR_001740023.2:n.3045dup
XR_245095.4:n.2871dup
NM_145262.4:c.*47dup MANE Select	NP_660305.2:n.*47dup
NR_026699.2:n.1709dup
NR_026700.2:n.815dup
NR_026701.2:n.1707dup
NR_026702.2:n.745dup
NM_001144951.2:c.*738dup	NP_001138423.1:n.*738dup