Canonical Allele Identifier: CA2665985129

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293204-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293204G>T , CM000665.2:g.52293204G>T	GRCh38
NC_000003.11:g.52327220G>T , CM000665.1:g.52327220G>T	GRCh37
NC_000003.10:g.52302260G>T	NCBI36
NG_023246.1:g.10385G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*78G>T MANE Select	ENSP00000389175.2:n.*78G>T
ENST00000436784.6:c.*78G>T	ENSP00000389175.2:n.*78G>T
ENST00000471180.5:c.*58+12G>T	ENSP00000417526.1:n.*58+12G>T
ENST00000473032.5:c.*58+12G>T	ENSP00000418951.1:n.*58+12G>T
ENST00000486393.5:c.*1013G>T	ENSP00000419868.1:n.*1013G>T
ENST00000489173.1:n.1914+30G>T
NM_145262.3:c.*78G>T	NP_660305.2:n.*78G>T
NR_026699.1:n.1748G>T
NR_026700.1:n.842+12G>T
NR_026701.1:n.1734+12G>T
NR_026702.1:n.772+12G>T
XM_005264878.2:c.*769G>T	XP_005264935.1:n.*769G>T
XR_245095.2:n.2889+12G>T
XM_017005730.1:c.*78G>T	XP_016861219.1:n.*78G>T
XM_024453351.1:c.*78G>T	XP_024309119.1:n.*78G>T
XM_024453352.1:c.*769G>T	XP_024309120.1:n.*769G>T
XR_001740022.2:n.3540+12G>T
XR_001740023.2:n.3064+12G>T
XR_245095.4:n.2890+12G>T
NM_145262.4:c.*78G>T MANE Select	NP_660305.2:n.*78G>T
NR_026699.2:n.1740G>T
NR_026700.2:n.834+12G>T
NR_026701.2:n.1726+12G>T
NR_026702.2:n.764+12G>T
NM_001144951.2:c.*769G>T	NP_001138423.1:n.*769G>T