Canonical Allele Identifier: CA2665985207

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293317-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293317A>T , CM000665.2:g.52293317A>T	GRCh38
NC_000003.11:g.52327333A>T , CM000665.1:g.52327333A>T	GRCh37
NC_000003.10:g.52302373A>T	NCBI36
NG_023246.1:g.10498A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*191A>T MANE Select	ENSP00000389175.2:n.*191A>T
ENST00000436784.6:c.*191A>T	ENSP00000389175.2:n.*191A>T
ENST00000471180.5:c.*69A>T	ENSP00000417526.1:n.*69A>T
ENST00000473032.5:c.*69A>T	ENSP00000418951.1:n.*69A>T
ENST00000486393.5:c.*1126A>T	ENSP00000419868.1:n.*1126A>T
ENST00000489173.1:n.1925A>T
NM_145262.3:c.*191A>T	NP_660305.2:n.*191A>T
NR_026699.1:n.1861A>T
NR_026700.1:n.853A>T
NR_026701.1:n.1745A>T
NR_026702.1:n.783A>T
XM_005264878.2:c.*882A>T	XP_005264935.1:n.*882A>T
XR_245095.2:n.2900A>T
XM_017005730.1:c.*191A>T	XP_016861219.1:n.*191A>T
XM_024453351.1:c.*191A>T	XP_024309119.1:n.*191A>T
XM_024453352.1:c.*882A>T	XP_024309120.1:n.*882A>T
XR_001740022.2:n.3551A>T
XR_001740023.2:n.3075A>T
XR_245095.4:n.2901A>T
NM_145262.4:c.*191A>T MANE Select	NP_660305.2:n.*191A>T
NR_026699.2:n.1853A>T
NR_026700.2:n.845A>T
NR_026701.2:n.1737A>T
NR_026702.2:n.775A>T
NM_001144951.2:c.*882A>T	NP_001138423.1:n.*882A>T