Canonical Allele Identifier: CA2577780417

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293203-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293206del , CM000665.2:g.52293206del	GRCh38
NC_000003.11:g.52327222del , CM000665.1:g.52327222del	GRCh37
NC_000003.10:g.52302262del	NCBI36
NG_023246.1:g.10387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*80del MANE Select	ENSP00000389175.2:n.*80del
ENST00000436784.6:c.*80del	ENSP00000389175.2:n.*80del
ENST00000471180.5:c.*58+14del	ENSP00000417526.1:n.*58+14del
ENST00000473032.5:c.*58+14del	ENSP00000418951.1:n.*58+14del
ENST00000486393.5:c.*1015del	ENSP00000419868.1:n.*1015del
ENST00000489173.1:n.1914+32del
NM_145262.3:c.*80del	NP_660305.2:n.*80del
NR_026699.1:n.1750del
NR_026700.1:n.842+14del
NR_026701.1:n.1734+14del
NR_026702.1:n.772+14del
XM_005264878.2:c.*771del	XP_005264935.1:n.*771del
XR_245095.2:n.2889+14del
XM_017005730.1:c.*80del	XP_016861219.1:n.*80del
XM_024453351.1:c.*80del	XP_024309119.1:n.*80del
XM_024453352.1:c.*771del	XP_024309120.1:n.*771del
XR_001740022.2:n.3540+14del
XR_001740023.2:n.3064+14del
XR_245095.4:n.2890+14del
NM_145262.4:c.*80del MANE Select	NP_660305.2:n.*80del
NR_026699.2:n.1742del
NR_026700.2:n.834+14del
NR_026701.2:n.1726+14del
NR_026702.2:n.764+14del
NM_001144951.2:c.*771del	NP_001138423.1:n.*771del