Canonical Allele Identifier: CA433882956

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326641C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292625C>T , CM000665.2:g.52292625C>T	GRCh38
NC_000003.11:g.52326641C>T , CM000665.1:g.52326641C>T	GRCh37
NC_000003.10:g.52301681C>T	NCBI36
NG_023246.1:g.9806C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1071C>T MANE Select	ENSP00000389175.2:p.Thr357=
ENST00000305690.12:c.*190C>T	ENSP00000301965.9:n.*190C>T
ENST00000436784.6:c.1071C>T	ENSP00000389175.2:p.Thr357=
ENST00000461183.5:c.763+56C>T	ENSP00000417264.1:n.763+56C>T
ENST00000471180.5:c.634+56C>T	ENSP00000417526.1:n.634+56C>T
ENST00000473032.5:c.530-421C>T	ENSP00000418951.1:n.530-421C>T
ENST00000477382.1:c.*190C>T	ENSP00000419008.1:n.*190C>T
ENST00000486393.5:c.*434C>T	ENSP00000419868.1:n.*434C>T
ENST00000489173.1:n.1365C>T
NM_001144951.1:c.*190C>T	NP_001138423.1:n.*190C>T
NM_145262.3:c.1071C>T	NP_660305.2:p.Thr357=
NR_026699.1:n.1169C>T
NR_026700.1:n.695+56C>T
NR_026701.1:n.1167C>T
NR_026702.1:n.626-421C>T
XM_005264878.2:c.*190C>T	XP_005264935.1:n.*190C>T
XR_245095.2:n.2742+56C>T
XM_017005730.1:c.690C>T	XP_016861219.1:p.Thr230=
XM_024453351.1:c.1071C>T	XP_024309119.1:p.Thr357=
XM_024453352.1:c.*190C>T	XP_024309120.1:n.*190C>T
XR_001740022.2:n.2973C>T
XR_001740023.2:n.2917+56C>T
XR_245095.4:n.2743+56C>T
NM_145262.4:c.1071C>T MANE Select	NP_660305.2:p.Thr357=
NR_026699.2:n.1161C>T
NR_026700.2:n.687+56C>T
NR_026701.2:n.1159C>T
NR_026702.2:n.618-421C>T
NM_001144951.2:c.*190C>T	NP_001138423.1:n.*190C>T