Canonical Allele Identifier: CA433752053

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327152T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293136T>G , CM000665.2:g.52293136T>G	GRCh38
NC_000003.11:g.52327152T>G , CM000665.1:g.52327152T>G	GRCh37
NC_000003.10:g.52302192T>G	NCBI36
NG_023246.1:g.10317T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*10T>G MANE Select	ENSP00000389175.2:n.*10T>G
ENST00000436784.6:c.*10T>G	ENSP00000389175.2:n.*10T>G
ENST00000461183.5:c.*2T>G	ENSP00000417264.1:n.*2T>G
ENST00000471180.5:c.*2T>G	ENSP00000417526.1:n.*2T>G
ENST00000473032.5:c.*2T>G	ENSP00000418951.1:n.*2T>G
ENST00000486393.5:c.*945T>G	ENSP00000419868.1:n.*945T>G
ENST00000489173.1:n.1876T>G
NM_145262.3:c.*10T>G	NP_660305.2:n.*10T>G
NR_026699.1:n.1680T>G
NR_026700.1:n.786T>G
NR_026701.1:n.1678T>G
NR_026702.1:n.716T>G
XM_005264878.2:c.*701T>G	XP_005264935.1:n.*701T>G
XR_245095.2:n.2833T>G
XM_017005730.1:c.*10T>G	XP_016861219.1:n.*10T>G
XM_024453351.1:c.*10T>G	XP_024309119.1:n.*10T>G
XM_024453352.1:c.*701T>G	XP_024309120.1:n.*701T>G
XR_001740022.2:n.3484T>G
XR_001740023.2:n.3008T>G
XR_245095.4:n.2834T>G
NM_145262.4:c.*10T>G MANE Select	NP_660305.2:n.*10T>G
NR_026699.2:n.1672T>G
NR_026700.2:n.778T>G
NR_026701.2:n.1670T>G
NR_026702.2:n.708T>G
NM_001144951.2:c.*701T>G	NP_001138423.1:n.*701T>G