Canonical Allele Identifier: CA353076787

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1559467394
• MyVariant Identifiers: chr3:g.52327112C>T (hg19) ; chr3:g.52293096C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293096C>T , CM000665.2:g.52293096C>T	GRCh38
NC_000003.11:g.52327112C>T , CM000665.1:g.52327112C>T	GRCh37
NC_000003.10:g.52302152C>T	NCBI36
NG_023246.1:g.10277C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1542C>T MANE Select	ENSP00000389175.2:p.Asp514=
ENST00000436784.6:c.1542C>T	ENSP00000389175.2:p.Asp514=
ENST00000461183.5:c.814C>T	ENSP00000417264.1:p.His272Tyr
ENST00000471180.5:c.685C>T	ENSP00000417526.1:p.His229Tyr
ENST00000473032.5:c.580C>T	ENSP00000418951.1:p.His194Tyr
ENST00000486393.5:c.*905C>T	ENSP00000419868.1:n.*905C>T
ENST00000489173.1:n.1836C>T
NM_145262.3:c.1542C>T	NP_660305.2:p.Asp514=
NR_026699.1:n.1640C>T
NR_026700.1:n.746C>T
NR_026701.1:n.1638C>T
NR_026702.1:n.676C>T
XM_005264878.2:c.*661C>T	XP_005264935.1:n.*661C>T
XR_245095.2:n.2793C>T
XM_017005730.1:c.1161C>T	XP_016861219.1:p.Asp387=
XM_024453351.1:c.1542C>T	XP_024309119.1:p.Asp514=
XM_024453352.1:c.*661C>T	XP_024309120.1:n.*661C>T
XR_001740022.2:n.3444C>T
XR_001740023.2:n.2968C>T
XR_245095.4:n.2794C>T
NM_145262.4:c.1542C>T MANE Select	NP_660305.2:p.Asp514=
NR_026699.2:n.1632C>T
NR_026700.2:n.738C>T
NR_026701.2:n.1630C>T
NR_026702.2:n.668C>T
NM_001144951.2:c.*661C>T	NP_001138423.1:n.*661C>T