Canonical Allele Identifier: CA433752008

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327013C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292997C>A , CM000665.2:g.52292997C>A	GRCh38
NC_000003.11:g.52327013C>A , CM000665.1:g.52327013C>A	GRCh37
NC_000003.10:g.52302053C>A	NCBI36
NG_023246.1:g.10178C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1443C>A MANE Select	ENSP00000389175.2:p.Ala481=
ENST00000305690.12:c.*562C>A	ENSP00000301965.9:n.*562C>A
ENST00000436784.6:c.1443C>A	ENSP00000389175.2:p.Ala481=
ENST00000461183.5:c.764-49C>A	ENSP00000417264.1:n.764-49C>A
ENST00000471180.5:c.635-49C>A	ENSP00000417526.1:n.635-49C>A
ENST00000473032.5:c.530-49C>A	ENSP00000418951.1:n.530-49C>A
ENST00000477382.1:c.*562C>A	ENSP00000419008.1:n.*562C>A
ENST00000486393.5:c.*806C>A	ENSP00000419868.1:n.*806C>A
ENST00000489173.1:n.1737C>A
NM_001144951.1:c.*562C>A	NP_001138423.1:n.*562C>A
NM_145262.3:c.1443C>A	NP_660305.2:p.Ala481=
NR_026699.1:n.1541C>A
NR_026700.1:n.696-49C>A
NR_026701.1:n.1539C>A
NR_026702.1:n.626-49C>A
XM_005264878.2:c.*562C>A	XP_005264935.1:n.*562C>A
XR_245095.2:n.2743-49C>A
XM_017005730.1:c.1062C>A	XP_016861219.1:p.Ala354=
XM_024453351.1:c.1443C>A	XP_024309119.1:p.Ala481=
XM_024453352.1:c.*562C>A	XP_024309120.1:n.*562C>A
XR_001740022.2:n.3345C>A
XR_001740023.2:n.2918-49C>A
XR_245095.4:n.2744-49C>A
NM_145262.4:c.1443C>A MANE Select	NP_660305.2:p.Ala481=
NR_026699.2:n.1533C>A
NR_026700.2:n.688-49C>A
NR_026701.2:n.1531C>A
NR_026702.2:n.618-49C>A
NM_001144951.2:c.*562C>A	NP_001138423.1:n.*562C>A