Canonical Allele Identifier: CA353076574

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327066G>T (hg19) ; chr3:g.52293050G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293050G>T , CM000665.2:g.52293050G>T	GRCh38
NC_000003.11:g.52327066G>T , CM000665.1:g.52327066G>T	GRCh37
NC_000003.10:g.52302106G>T	NCBI36
NG_023246.1:g.10231G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1496G>T MANE Select	ENSP00000389175.2:p.Gly499Val
ENST00000436784.6:c.1496G>T	ENSP00000389175.2:p.Gly499Val
ENST00000461183.5:c.768G>T	ENSP00000417264.1:p.Trp256Cys
ENST00000471180.5:c.639G>T	ENSP00000417526.1:p.Trp213Cys
ENST00000473032.5:c.534G>T	ENSP00000418951.1:p.Trp178Cys
ENST00000486393.5:c.*859G>T	ENSP00000419868.1:n.*859G>T
ENST00000489173.1:n.1790G>T
NM_145262.3:c.1496G>T	NP_660305.2:p.Gly499Val
NR_026699.1:n.1594G>T
NR_026700.1:n.700G>T
NR_026701.1:n.1592G>T
NR_026702.1:n.630G>T
XM_005264878.2:c.*615G>T	XP_005264935.1:n.*615G>T
XR_245095.2:n.2747G>T
XM_017005730.1:c.1115G>T	XP_016861219.1:p.Gly372Val
XM_024453351.1:c.1496G>T	XP_024309119.1:p.Gly499Val
XM_024453352.1:c.*615G>T	XP_024309120.1:n.*615G>T
XR_001740022.2:n.3398G>T
XR_001740023.2:n.2922G>T
XR_245095.4:n.2748G>T
NM_145262.4:c.1496G>T MANE Select	NP_660305.2:p.Gly499Val
NR_026699.2:n.1586G>T
NR_026700.2:n.692G>T
NR_026701.2:n.1584G>T
NR_026702.2:n.622G>T
NM_001144951.2:c.*615G>T	NP_001138423.1:n.*615G>T