Canonical Allele Identifier: CA353076789

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327113A>C (hg19) ; chr3:g.52293097A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293097A>C , CM000665.2:g.52293097A>C	GRCh38
NC_000003.11:g.52327113A>C , CM000665.1:g.52327113A>C	GRCh37
NC_000003.10:g.52302153A>C	NCBI36
NG_023246.1:g.10278A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1543A>C MANE Select	ENSP00000389175.2:p.Thr515Pro
ENST00000436784.6:c.1543A>C	ENSP00000389175.2:p.Thr515Pro
ENST00000461183.5:c.815A>C	ENSP00000417264.1:p.His272Pro
ENST00000471180.5:c.686A>C	ENSP00000417526.1:p.His229Pro
ENST00000473032.5:c.581A>C	ENSP00000418951.1:p.His194Pro
ENST00000486393.5:c.*906A>C	ENSP00000419868.1:n.*906A>C
ENST00000489173.1:n.1837A>C
NM_145262.3:c.1543A>C	NP_660305.2:p.Thr515Pro
NR_026699.1:n.1641A>C
NR_026700.1:n.747A>C
NR_026701.1:n.1639A>C
NR_026702.1:n.677A>C
XM_005264878.2:c.*662A>C	XP_005264935.1:n.*662A>C
XR_245095.2:n.2794A>C
XM_017005730.1:c.1162A>C	XP_016861219.1:p.Thr388Pro
XM_024453351.1:c.1543A>C	XP_024309119.1:p.Thr515Pro
XM_024453352.1:c.*662A>C	XP_024309120.1:n.*662A>C
XR_001740022.2:n.3445A>C
XR_001740023.2:n.2969A>C
XR_245095.4:n.2795A>C
NM_145262.4:c.1543A>C MANE Select	NP_660305.2:p.Thr515Pro
NR_026699.2:n.1633A>C
NR_026700.2:n.739A>C
NR_026701.2:n.1631A>C
NR_026702.2:n.669A>C
NM_001144951.2:c.*662A>C	NP_001138423.1:n.*662A>C