Canonical Allele Identifier: CA353076819

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327118C>A (hg19) ; chr3:g.52293102C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293102C>A , CM000665.2:g.52293102C>A	GRCh38
NC_000003.11:g.52327118C>A , CM000665.1:g.52327118C>A	GRCh37
NC_000003.10:g.52302158C>A	NCBI36
NG_023246.1:g.10283C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1548C>A MANE Select	ENSP00000389175.2:p.His516Gln
ENST00000436784.6:c.1548C>A	ENSP00000389175.2:p.His516Gln
ENST00000461183.5:c.820C>A	ENSP00000417264.1:p.Pro274Thr
ENST00000471180.5:c.691C>A	ENSP00000417526.1:p.Pro231Thr
ENST00000473032.5:c.586C>A	ENSP00000418951.1:p.Pro196Thr
ENST00000486393.5:c.*911C>A	ENSP00000419868.1:n.*911C>A
ENST00000489173.1:n.1842C>A
NM_145262.3:c.1548C>A	NP_660305.2:p.His516Gln
NR_026699.1:n.1646C>A
NR_026700.1:n.752C>A
NR_026701.1:n.1644C>A
NR_026702.1:n.682C>A
XM_005264878.2:c.*667C>A	XP_005264935.1:n.*667C>A
XR_245095.2:n.2799C>A
XM_017005730.1:c.1167C>A	XP_016861219.1:p.His389Gln
XM_024453351.1:c.1548C>A	XP_024309119.1:p.His516Gln
XM_024453352.1:c.*667C>A	XP_024309120.1:n.*667C>A
XR_001740022.2:n.3450C>A
XR_001740023.2:n.2974C>A
XR_245095.4:n.2800C>A
NM_145262.4:c.1548C>A MANE Select	NP_660305.2:p.His516Gln
NR_026699.2:n.1638C>A
NR_026700.2:n.744C>A
NR_026701.2:n.1636C>A
NR_026702.2:n.674C>A
NM_001144951.2:c.*667C>A	NP_001138423.1:n.*667C>A