Canonical Allele Identifier: CA353076647

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327086G>T (hg19) ; chr3:g.52293070G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293070G>T , CM000665.2:g.52293070G>T	GRCh38
NC_000003.11:g.52327086G>T , CM000665.1:g.52327086G>T	GRCh37
NC_000003.10:g.52302126G>T	NCBI36
NG_023246.1:g.10251G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1516G>T MANE Select	ENSP00000389175.2:p.Gly506Trp
ENST00000436784.6:c.1516G>T	ENSP00000389175.2:p.Gly506Trp
ENST00000461183.5:c.788G>T	ENSP00000417264.1:p.Arg263Met
ENST00000471180.5:c.659G>T	ENSP00000417526.1:p.Arg220Met
ENST00000473032.5:c.554G>T	ENSP00000418951.1:p.Arg185Met
ENST00000486393.5:c.*879G>T	ENSP00000419868.1:n.*879G>T
ENST00000489173.1:n.1810G>T
NM_145262.3:c.1516G>T	NP_660305.2:p.Gly506Trp
NR_026699.1:n.1614G>T
NR_026700.1:n.720G>T
NR_026701.1:n.1612G>T
NR_026702.1:n.650G>T
XM_005264878.2:c.*635G>T	XP_005264935.1:n.*635G>T
XR_245095.2:n.2767G>T
XM_017005730.1:c.1135G>T	XP_016861219.1:p.Gly379Trp
XM_024453351.1:c.1516G>T	XP_024309119.1:p.Gly506Trp
XM_024453352.1:c.*635G>T	XP_024309120.1:n.*635G>T
XR_001740022.2:n.3418G>T
XR_001740023.2:n.2942G>T
XR_245095.4:n.2768G>T
NM_145262.4:c.1516G>T MANE Select	NP_660305.2:p.Gly506Trp
NR_026699.2:n.1606G>T
NR_026700.2:n.712G>T
NR_026701.2:n.1604G>T
NR_026702.2:n.642G>T
NM_001144951.2:c.*635G>T	NP_001138423.1:n.*635G>T