Canonical Allele Identifier: CA433882991

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326665G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292649G>A , CM000665.2:g.52292649G>A	GRCh38
NC_000003.11:g.52326665G>A , CM000665.1:g.52326665G>A	GRCh37
NC_000003.10:g.52301705G>A	NCBI36
NG_023246.1:g.9830G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1095G>A MANE Select	ENSP00000389175.2:p.Gly365=
ENST00000305690.12:c.*214G>A	ENSP00000301965.9:n.*214G>A
ENST00000436784.6:c.1095G>A	ENSP00000389175.2:p.Gly365=
ENST00000461183.5:c.763+80G>A	ENSP00000417264.1:n.763+80G>A
ENST00000471180.5:c.634+80G>A	ENSP00000417526.1:n.634+80G>A
ENST00000473032.5:c.530-397G>A	ENSP00000418951.1:n.530-397G>A
ENST00000477382.1:c.*214G>A	ENSP00000419008.1:n.*214G>A
ENST00000486393.5:c.*458G>A	ENSP00000419868.1:n.*458G>A
ENST00000489173.1:n.1389G>A
NM_001144951.1:c.*214G>A	NP_001138423.1:n.*214G>A
NM_145262.3:c.1095G>A	NP_660305.2:p.Gly365=
NR_026699.1:n.1193G>A
NR_026700.1:n.695+80G>A
NR_026701.1:n.1191G>A
NR_026702.1:n.626-397G>A
XM_005264878.2:c.*214G>A	XP_005264935.1:n.*214G>A
XR_245095.2:n.2742+80G>A
XM_017005730.1:c.714G>A	XP_016861219.1:p.Gly238=
XM_024453351.1:c.1095G>A	XP_024309119.1:p.Gly365=
XM_024453352.1:c.*214G>A	XP_024309120.1:n.*214G>A
XR_001740022.2:n.2997G>A
XR_001740023.2:n.2917+80G>A
XR_245095.4:n.2743+80G>A
NM_145262.4:c.1095G>A MANE Select	NP_660305.2:p.Gly365=
NR_026699.2:n.1185G>A
NR_026700.2:n.687+80G>A
NR_026701.2:n.1183G>A
NR_026702.2:n.618-397G>A
NM_001144951.2:c.*214G>A	NP_001138423.1:n.*214G>A