Canonical Allele Identifier: CA353075979

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326936G>T (hg19) ; chr3:g.52292920G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292920G>T , CM000665.2:g.52292920G>T	GRCh38
NC_000003.11:g.52326936G>T , CM000665.1:g.52326936G>T	GRCh37
NC_000003.10:g.52301976G>T	NCBI36
NG_023246.1:g.10101G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1366G>T MANE Select	ENSP00000389175.2:p.Gly456Trp
ENST00000305690.12:c.*485G>T	ENSP00000301965.9:n.*485G>T
ENST00000436784.6:c.1366G>T	ENSP00000389175.2:p.Gly456Trp
ENST00000461183.5:c.764-126G>T	ENSP00000417264.1:n.764-126G>T
ENST00000471180.5:c.635-126G>T	ENSP00000417526.1:n.635-126G>T
ENST00000473032.5:c.530-126G>T	ENSP00000418951.1:n.530-126G>T
ENST00000477382.1:c.*485G>T	ENSP00000419008.1:n.*485G>T
ENST00000486393.5:c.*729G>T	ENSP00000419868.1:n.*729G>T
ENST00000489173.1:n.1660G>T
NM_001144951.1:c.*485G>T	NP_001138423.1:n.*485G>T
NM_145262.3:c.1366G>T	NP_660305.2:p.Gly456Trp
NR_026699.1:n.1464G>T
NR_026700.1:n.696-126G>T
NR_026701.1:n.1462G>T
NR_026702.1:n.626-126G>T
XM_005264878.2:c.*485G>T	XP_005264935.1:n.*485G>T
XR_245095.2:n.2743-126G>T
XM_017005730.1:c.985G>T	XP_016861219.1:p.Gly329Trp
XM_024453351.1:c.1366G>T	XP_024309119.1:p.Gly456Trp
XM_024453352.1:c.*485G>T	XP_024309120.1:n.*485G>T
XR_001740022.2:n.3268G>T
XR_001740023.2:n.2918-126G>T
XR_245095.4:n.2744-126G>T
NM_145262.4:c.1366G>T MANE Select	NP_660305.2:p.Gly456Trp
NR_026699.2:n.1456G>T
NR_026700.2:n.688-126G>T
NR_026701.2:n.1454G>T
NR_026702.2:n.618-126G>T
NM_001144951.2:c.*485G>T	NP_001138423.1:n.*485G>T