Canonical Allele Identifier: CA2756266618

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293253G>T , CM000665.2:g.52293253G>T	GRCh38
NC_000003.11:g.52327269G>T , CM000665.1:g.52327269G>T	GRCh37
NC_000003.10:g.52302309G>T	NCBI36
NG_023246.1:g.10434G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*127G>T MANE Select	ENSP00000389175.2:n.*127G>T
ENST00000436784.6:c.*127G>T	ENSP00000389175.2:n.*127G>T
ENST00000471180.5:c.*59-54G>T	ENSP00000417526.1:n.*59-54G>T
ENST00000473032.5:c.*59-54G>T	ENSP00000418951.1:n.*59-54G>T
ENST00000486393.5:c.*1062G>T	ENSP00000419868.1:n.*1062G>T
ENST00000489173.1:n.1915-54G>T
NM_145262.3:c.*127G>T	NP_660305.2:n.*127G>T
NR_026699.1:n.1797G>T
NR_026700.1:n.843-54G>T
NR_026701.1:n.1735-54G>T
NR_026702.1:n.773-54G>T
XM_005264878.2:c.*818G>T	XP_005264935.1:n.*818G>T
XR_245095.2:n.2890-54G>T
XM_017005730.1:c.*127G>T	XP_016861219.1:n.*127G>T
XM_024453351.1:c.*127G>T	XP_024309119.1:n.*127G>T
XM_024453352.1:c.*818G>T	XP_024309120.1:n.*818G>T
XR_001740022.2:n.3541-54G>T
XR_001740023.2:n.3065-54G>T
XR_245095.4:n.2891-54G>T
NM_145262.4:c.*127G>T MANE Select	NP_660305.2:n.*127G>T
NR_026699.2:n.1789G>T
NR_026700.2:n.835-54G>T
NR_026701.2:n.1727-54G>T
NR_026702.2:n.765-54G>T
NM_001144951.2:c.*818G>T	NP_001138423.1:n.*818G>T