Canonical Allele Identifier: CA353076727

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327101A>G (hg19) ; chr3:g.52293085A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293085A>G , CM000665.2:g.52293085A>G	GRCh38
NC_000003.11:g.52327101A>G , CM000665.1:g.52327101A>G	GRCh37
NC_000003.10:g.52302141A>G	NCBI36
NG_023246.1:g.10266A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1531A>G MANE Select	ENSP00000389175.2:p.Asn511Asp
ENST00000436784.6:c.1531A>G	ENSP00000389175.2:p.Asn511Asp
ENST00000461183.5:c.803A>G	ENSP00000417264.1:p.Gln268Arg
ENST00000471180.5:c.674A>G	ENSP00000417526.1:p.Gln225Arg
ENST00000473032.5:c.569A>G	ENSP00000418951.1:p.Gln190Arg
ENST00000486393.5:c.*894A>G	ENSP00000419868.1:n.*894A>G
ENST00000489173.1:n.1825A>G
NM_145262.3:c.1531A>G	NP_660305.2:p.Asn511Asp
NR_026699.1:n.1629A>G
NR_026700.1:n.735A>G
NR_026701.1:n.1627A>G
NR_026702.1:n.665A>G
XM_005264878.2:c.*650A>G	XP_005264935.1:n.*650A>G
XR_245095.2:n.2782A>G
XM_017005730.1:c.1150A>G	XP_016861219.1:p.Asn384Asp
XM_024453351.1:c.1531A>G	XP_024309119.1:p.Asn511Asp
XM_024453352.1:c.*650A>G	XP_024309120.1:n.*650A>G
XR_001740022.2:n.3433A>G
XR_001740023.2:n.2957A>G
XR_245095.4:n.2783A>G
NM_145262.4:c.1531A>G MANE Select	NP_660305.2:p.Asn511Asp
NR_026699.2:n.1621A>G
NR_026700.2:n.727A>G
NR_026701.2:n.1619A>G
NR_026702.2:n.657A>G
NM_001144951.2:c.*650A>G	NP_001138423.1:n.*650A>G