Canonical Allele Identifier: CA1364789256

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293110_52293111delinsTC , CM000665.2:g.52293110_52293111delinsTC	GRCh38
NC_000003.11:g.52327126_52327127delinsTC , CM000665.1:g.52327126_52327127delinsTC	GRCh37
NC_000003.10:g.52302166_52302167delinsTC	NCBI36
NG_023246.1:g.10291_10292delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1556_1557delinsTC MANE Select	ENSP00000389175.2:p.Phe519=
ENST00000436784.6:c.1556_1557delinsTC	ENSP00000389175.2:p.Phe519=
ENST00000461183.5:c.828_829delinsTC	ENSP00000417264.1:p.Val276=
ENST00000471180.5:c.699_700delinsTC	ENSP00000417526.1:p.Val233=
ENST00000473032.5:c.594_595delinsTC	ENSP00000418951.1:p.Val198=
ENST00000486393.5:c.*919_*920delinsTC	ENSP00000419868.1:n.*919_*920delinsTC
ENST00000489173.1:n.1850_1851delinsTC
NM_145262.3:c.1556_1557delinsTC	NP_660305.2:p.Phe519=
NR_026699.1:n.1654_1655delinsTC
NR_026700.1:n.760_761delinsTC
NR_026701.1:n.1652_1653delinsTC
NR_026702.1:n.690_691delinsTC
XM_005264878.2:c.*675_*676delinsTC	XP_005264935.1:n.*675_*676delinsTC
XR_245095.2:n.2807_2808delinsTC
XM_017005730.1:c.1175_1176delinsTC	XP_016861219.1:p.Phe392=
XM_024453351.1:c.1556_1557delinsTC	XP_024309119.1:p.Phe519=
XM_024453352.1:c.*675_*676delinsTC	XP_024309120.1:n.*675_*676delinsTC
XR_001740022.2:n.3458_3459delinsTC
XR_001740023.2:n.2982_2983delinsTC
XR_245095.4:n.2808_2809delinsTC
NM_145262.4:c.1556_1557delinsTC MANE Select	NP_660305.2:p.Phe519=
NR_026699.2:n.1646_1647delinsTC
NR_026700.2:n.752_753delinsTC
NR_026701.2:n.1644_1645delinsTC
NR_026702.2:n.682_683delinsTC
NM_001144951.2:c.*675_*676delinsTC	NP_001138423.1:n.*675_*676delinsTC