Canonical Allele Identifier: CA433752033

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327055C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293039C>T , CM000665.2:g.52293039C>T	GRCh38
NC_000003.11:g.52327055C>T , CM000665.1:g.52327055C>T	GRCh37
NC_000003.10:g.52302095C>T	NCBI36
NG_023246.1:g.10220C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1485C>T MANE Select	ENSP00000389175.2:p.Cys495=
ENST00000436784.6:c.1485C>T	ENSP00000389175.2:p.Cys495=
ENST00000461183.5:c.764-7C>T	ENSP00000417264.1:n.764-7C>T
ENST00000471180.5:c.635-7C>T	ENSP00000417526.1:n.635-7C>T
ENST00000473032.5:c.530-7C>T	ENSP00000418951.1:n.530-7C>T
ENST00000486393.5:c.*848C>T	ENSP00000419868.1:n.*848C>T
ENST00000489173.1:n.1779C>T
NM_145262.3:c.1485C>T	NP_660305.2:p.Cys495=
NR_026699.1:n.1583C>T
NR_026700.1:n.696-7C>T
NR_026701.1:n.1581C>T
NR_026702.1:n.626-7C>T
XM_005264878.2:c.*604C>T	XP_005264935.1:n.*604C>T
XR_245095.2:n.2743-7C>T
XM_017005730.1:c.1104C>T	XP_016861219.1:p.Cys368=
XM_024453351.1:c.1485C>T	XP_024309119.1:p.Cys495=
XM_024453352.1:c.*604C>T	XP_024309120.1:n.*604C>T
XR_001740022.2:n.3387C>T
XR_001740023.2:n.2918-7C>T
XR_245095.4:n.2744-7C>T
NM_145262.4:c.1485C>T MANE Select	NP_660305.2:p.Cys495=
NR_026699.2:n.1575C>T
NR_026700.2:n.688-7C>T
NR_026701.2:n.1573C>T
NR_026702.2:n.618-7C>T
NM_001144951.2:c.*604C>T	NP_001138423.1:n.*604C>T