Canonical Allele Identifier: CA353076960

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327142A>G (hg19) ; chr3:g.52293126A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293126A>G , CM000665.2:g.52293126A>G	GRCh38
NC_000003.11:g.52327142A>G , CM000665.1:g.52327142A>G	GRCh37
NC_000003.10:g.52302182A>G	NCBI36
NG_023246.1:g.10307A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1572A>G MANE Select	ENSP00000389175.2:p.Ter524Trp
ENST00000436784.6:c.1572A>G	ENSP00000389175.2:p.Ter524Trp
ENST00000461183.5:c.844A>G	ENSP00000417264.1:p.Met282Val
ENST00000471180.5:c.715A>G	ENSP00000417526.1:p.Met239Val
ENST00000473032.5:c.610A>G	ENSP00000418951.1:p.Met204Val
ENST00000486393.5:c.*935A>G	ENSP00000419868.1:n.*935A>G
ENST00000489173.1:n.1866A>G
NM_145262.3:c.1572A>G	NP_660305.2:p.Ter524Trp
NR_026699.1:n.1670A>G
NR_026700.1:n.776A>G
NR_026701.1:n.1668A>G
NR_026702.1:n.706A>G
XM_005264878.2:c.*691A>G	XP_005264935.1:n.*691A>G
XR_245095.2:n.2823A>G
XM_017005730.1:c.1191A>G	XP_016861219.1:p.Ter397Trp
XM_024453351.1:c.1572A>G	XP_024309119.1:p.Ter524Trp
XM_024453352.1:c.*691A>G	XP_024309120.1:n.*691A>G
XR_001740022.2:n.3474A>G
XR_001740023.2:n.2998A>G
XR_245095.4:n.2824A>G
NM_145262.4:c.1572A>G MANE Select	NP_660305.2:p.Ter524Trp
NR_026699.2:n.1662A>G
NR_026700.2:n.768A>G
NR_026701.2:n.1660A>G
NR_026702.2:n.698A>G
NM_001144951.2:c.*691A>G	NP_001138423.1:n.*691A>G