Canonical Allele Identifier: CA353076703

Gene: GLYCTK

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1527T>A MANE Select	ENSP00000389175.2:p.Gly509=
ENST00000436784.6:c.1527T>A	ENSP00000389175.2:p.Gly509=
ENST00000461183.5:c.799T>A	ENSP00000417264.1:p.Tyr267Asn
ENST00000471180.5:c.670T>A	ENSP00000417526.1:p.Tyr224Asn
ENST00000473032.5:c.565T>A	ENSP00000418951.1:p.Tyr189Asn
ENST00000486393.5:c.*890T>A	ENSP00000419868.1:n.*890T>A
ENST00000489173.1:n.1821T>A
NM_145262.3:c.1527T>A	NP_660305.2:p.Gly509=
NR_026699.1:n.1625T>A
NR_026700.1:n.731T>A
NR_026701.1:n.1623T>A
NR_026702.1:n.661T>A
XM_005264878.2:c.*646T>A	XP_005264935.1:n.*646T>A
XR_245095.2:n.2778T>A
XM_017005730.1:c.1146T>A	XP_016861219.1:p.Gly382=
XM_024453351.1:c.1527T>A	XP_024309119.1:p.Gly509=
XM_024453352.1:c.*646T>A	XP_024309120.1:n.*646T>A
XR_001740022.2:n.3429T>A
XR_001740023.2:n.2953T>A
XR_245095.4:n.2779T>A
NM_145262.4:c.1527T>A MANE Select	NP_660305.2:p.Gly509=
NR_026699.2:n.1617T>A
NR_026700.2:n.723T>A
NR_026701.2:n.1615T>A
NR_026702.2:n.653T>A
NM_001144951.2:c.*646T>A	NP_001138423.1:n.*646T>A