Canonical Allele Identifier: CA433752036

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327058C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293042C>T , CM000665.2:g.52293042C>T	GRCh38
NC_000003.11:g.52327058C>T , CM000665.1:g.52327058C>T	GRCh37
NC_000003.10:g.52302098C>T	NCBI36
NG_023246.1:g.10223C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1488C>T MANE Select	ENSP00000389175.2:p.Leu496=
ENST00000436784.6:c.1488C>T	ENSP00000389175.2:p.Leu496=
ENST00000461183.5:c.764-4C>T	ENSP00000417264.1:n.764-4C>T
ENST00000471180.5:c.635-4C>T	ENSP00000417526.1:n.635-4C>T
ENST00000473032.5:c.530-4C>T	ENSP00000418951.1:n.530-4C>T
ENST00000486393.5:c.*851C>T	ENSP00000419868.1:n.*851C>T
ENST00000489173.1:n.1782C>T
NM_145262.3:c.1488C>T	NP_660305.2:p.Leu496=
NR_026699.1:n.1586C>T
NR_026700.1:n.696-4C>T
NR_026701.1:n.1584C>T
NR_026702.1:n.626-4C>T
XM_005264878.2:c.*607C>T	XP_005264935.1:n.*607C>T
XR_245095.2:n.2743-4C>T
XM_017005730.1:c.1107C>T	XP_016861219.1:p.Leu369=
XM_024453351.1:c.1488C>T	XP_024309119.1:p.Leu496=
XM_024453352.1:c.*607C>T	XP_024309120.1:n.*607C>T
XR_001740022.2:n.3390C>T
XR_001740023.2:n.2918-4C>T
XR_245095.4:n.2744-4C>T
NM_145262.4:c.1488C>T MANE Select	NP_660305.2:p.Leu496=
NR_026699.2:n.1578C>T
NR_026700.2:n.688-4C>T
NR_026701.2:n.1576C>T
NR_026702.2:n.618-4C>T
NM_001144951.2:c.*607C>T	NP_001138423.1:n.*607C>T