Canonical Allele Identifier: CA2665985212

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293322-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293322G>A , CM000665.2:g.52293322G>A	GRCh38
NC_000003.11:g.52327338G>A , CM000665.1:g.52327338G>A	GRCh37
NC_000003.10:g.52302378G>A	NCBI36
NG_023246.1:g.10503G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*196G>A MANE Select	ENSP00000389175.2:n.*196G>A
ENST00000436784.6:c.*196G>A	ENSP00000389175.2:n.*196G>A
ENST00000471180.5:c.*74G>A	ENSP00000417526.1:n.*74G>A
ENST00000473032.5:c.*74G>A	ENSP00000418951.1:n.*74G>A
ENST00000486393.5:c.*1131G>A	ENSP00000419868.1:n.*1131G>A
ENST00000489173.1:n.1930G>A
NM_145262.3:c.*196G>A	NP_660305.2:n.*196G>A
NR_026699.1:n.1866G>A
NR_026700.1:n.858G>A
NR_026701.1:n.1750G>A
NR_026702.1:n.788G>A
XM_005264878.2:c.*887G>A	XP_005264935.1:n.*887G>A
XR_245095.2:n.2905G>A
XM_017005730.1:c.*196G>A	XP_016861219.1:n.*196G>A
XM_024453351.1:c.*196G>A	XP_024309119.1:n.*196G>A
XM_024453352.1:c.*887G>A	XP_024309120.1:n.*887G>A
XR_001740022.2:n.3556G>A
XR_001740023.2:n.3080G>A
XR_245095.4:n.2906G>A
NM_145262.4:c.*196G>A MANE Select	NP_660305.2:n.*196G>A
NR_026699.2:n.1858G>A
NR_026700.2:n.850G>A
NR_026701.2:n.1742G>A
NR_026702.2:n.780G>A
NM_001144951.2:c.*887G>A	NP_001138423.1:n.*887G>A