Canonical Allele Identifier: CA2838686287

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293052dup , CM000665.2:g.52293052dup	GRCh38
NC_000003.11:g.52327068dup , CM000665.1:g.52327068dup	GRCh37
NC_000003.10:g.52302108dup	NCBI36
NG_023246.1:g.10233dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1498dup MANE Select	ENSP00000389175.2:p.Ala500GlyfsTer28
ENST00000436784.6:c.1498dup	ENSP00000389175.2:p.Ala500GlyfsTer28
ENST00000461183.5:c.770dup	ENSP00000417264.1:p.Thr258HisfsTer8
ENST00000471180.5:c.641dup	ENSP00000417526.1:p.Thr215HisfsTer8
ENST00000473032.5:c.536dup	ENSP00000418951.1:p.Thr180HisfsTer8
ENST00000486393.5:c.*861dup	ENSP00000419868.1:n.*861dup
ENST00000489173.1:n.1792dup
NM_145262.3:c.1498dup	NP_660305.2:p.Ala500GlyfsTer28
NR_026699.1:n.1596dup
NR_026700.1:n.702dup
NR_026701.1:n.1594dup
NR_026702.1:n.632dup
XM_005264878.2:c.*617dup	XP_005264935.1:n.*617dup
XR_245095.2:n.2749dup
XM_017005730.1:c.1117dup	XP_016861219.1:p.Ala373GlyfsTer28
XM_024453351.1:c.1498dup	XP_024309119.1:p.Ala500GlyfsTer28
XM_024453352.1:c.*617dup	XP_024309120.1:n.*617dup
XR_001740022.2:n.3400dup
XR_001740023.2:n.2924dup
XR_245095.4:n.2750dup
NM_145262.4:c.1498dup MANE Select	NP_660305.2:p.Ala500GlyfsTer28
NR_026699.2:n.1588dup
NR_026700.2:n.694dup
NR_026701.2:n.1586dup
NR_026702.2:n.624dup
NM_001144951.2:c.*617dup	NP_001138423.1:n.*617dup