Canonical Allele Identifier: CA353076705

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327097T>G (hg19) ; chr3:g.52293081T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293081T>G , CM000665.2:g.52293081T>G	GRCh38
NC_000003.11:g.52327097T>G , CM000665.1:g.52327097T>G	GRCh37
NC_000003.10:g.52302137T>G	NCBI36
NG_023246.1:g.10262T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1527T>G MANE Select	ENSP00000389175.2:p.Gly509=
ENST00000436784.6:c.1527T>G	ENSP00000389175.2:p.Gly509=
ENST00000461183.5:c.799T>G	ENSP00000417264.1:p.Tyr267Asp
ENST00000471180.5:c.670T>G	ENSP00000417526.1:p.Tyr224Asp
ENST00000473032.5:c.565T>G	ENSP00000418951.1:p.Tyr189Asp
ENST00000486393.5:c.*890T>G	ENSP00000419868.1:n.*890T>G
ENST00000489173.1:n.1821T>G
NM_145262.3:c.1527T>G	NP_660305.2:p.Gly509=
NR_026699.1:n.1625T>G
NR_026700.1:n.731T>G
NR_026701.1:n.1623T>G
NR_026702.1:n.661T>G
XM_005264878.2:c.*646T>G	XP_005264935.1:n.*646T>G
XR_245095.2:n.2778T>G
XM_017005730.1:c.1146T>G	XP_016861219.1:p.Gly382=
XM_024453351.1:c.1527T>G	XP_024309119.1:p.Gly509=
XM_024453352.1:c.*646T>G	XP_024309120.1:n.*646T>G
XR_001740022.2:n.3429T>G
XR_001740023.2:n.2953T>G
XR_245095.4:n.2779T>G
NM_145262.4:c.1527T>G MANE Select	NP_660305.2:p.Gly509=
NR_026699.2:n.1617T>G
NR_026700.2:n.723T>G
NR_026701.2:n.1615T>G
NR_026702.2:n.653T>G
NM_001144951.2:c.*646T>G	NP_001138423.1:n.*646T>G