Canonical Allele Identifier: CA2665985161

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293249-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293249G>T , CM000665.2:g.52293249G>T	GRCh38
NC_000003.11:g.52327265G>T , CM000665.1:g.52327265G>T	GRCh37
NC_000003.10:g.52302305G>T	NCBI36
NG_023246.1:g.10430G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*123G>T MANE Select	ENSP00000389175.2:n.*123G>T
ENST00000436784.6:c.*123G>T	ENSP00000389175.2:n.*123G>T
ENST00000471180.5:c.*59-58G>T	ENSP00000417526.1:n.*59-58G>T
ENST00000473032.5:c.*59-58G>T	ENSP00000418951.1:n.*59-58G>T
ENST00000486393.5:c.*1058G>T	ENSP00000419868.1:n.*1058G>T
ENST00000489173.1:n.1915-58G>T
NM_145262.3:c.*123G>T	NP_660305.2:n.*123G>T
NR_026699.1:n.1793G>T
NR_026700.1:n.843-58G>T
NR_026701.1:n.1735-58G>T
NR_026702.1:n.773-58G>T
XM_005264878.2:c.*814G>T	XP_005264935.1:n.*814G>T
XR_245095.2:n.2890-58G>T
XM_017005730.1:c.*123G>T	XP_016861219.1:n.*123G>T
XM_024453351.1:c.*123G>T	XP_024309119.1:n.*123G>T
XM_024453352.1:c.*814G>T	XP_024309120.1:n.*814G>T
XR_001740022.2:n.3541-58G>T
XR_001740023.2:n.3065-58G>T
XR_245095.4:n.2891-58G>T
NM_145262.4:c.*123G>T MANE Select	NP_660305.2:n.*123G>T
NR_026699.2:n.1785G>T
NR_026700.2:n.835-58G>T
NR_026701.2:n.1727-58G>T
NR_026702.2:n.765-58G>T
NM_001144951.2:c.*814G>T	NP_001138423.1:n.*814G>T