Canonical Allele Identifier: CA1364789329

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1559467596
• gnomAD v4: 3-52293238-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293238T>C , CM000665.2:g.52293238T>C	GRCh38
NC_000003.11:g.52327254T>C , CM000665.1:g.52327254T>C	GRCh37
NC_000003.10:g.52302294T>C	NCBI36
NG_023246.1:g.10419T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*112T>C MANE Select	ENSP00000389175.2:n.*112T>C
ENST00000436784.6:c.*112T>C	ENSP00000389175.2:n.*112T>C
ENST00000471180.5:c.*58+46T>C	ENSP00000417526.1:n.*58+46T>C
ENST00000473032.5:c.*58+46T>C	ENSP00000418951.1:n.*58+46T>C
ENST00000486393.5:c.*1047T>C	ENSP00000419868.1:n.*1047T>C
ENST00000489173.1:n.1914+64T>C
NM_145262.3:c.*112T>C	NP_660305.2:n.*112T>C
NR_026699.1:n.1782T>C
NR_026700.1:n.842+46T>C
NR_026701.1:n.1734+46T>C
NR_026702.1:n.772+46T>C
XM_005264878.2:c.*803T>C	XP_005264935.1:n.*803T>C
XR_245095.2:n.2889+46T>C
XM_017005730.1:c.*112T>C	XP_016861219.1:n.*112T>C
XM_024453351.1:c.*112T>C	XP_024309119.1:n.*112T>C
XM_024453352.1:c.*803T>C	XP_024309120.1:n.*803T>C
XR_001740022.2:n.3540+46T>C
XR_001740023.2:n.3064+46T>C
XR_245095.4:n.2890+46T>C
NM_145262.4:c.*112T>C MANE Select	NP_660305.2:n.*112T>C
NR_026699.2:n.1774T>C
NR_026700.2:n.834+46T>C
NR_026701.2:n.1726+46T>C
NR_026702.2:n.764+46T>C
NM_001144951.2:c.*803T>C	NP_001138423.1:n.*803T>C