Canonical Allele Identifier: CA353075701

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52292851-G-T
• MyVariant Identifiers: chr3:g.52326867G>T (hg19) ; chr3:g.52292851G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292851G>T , CM000665.2:g.52292851G>T	GRCh38
NC_000003.11:g.52326867G>T , CM000665.1:g.52326867G>T	GRCh37
NC_000003.10:g.52301907G>T	NCBI36
NG_023246.1:g.10032G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1297G>T MANE Select	ENSP00000389175.2:p.Glu433Ter
ENST00000305690.12:c.*416G>T	ENSP00000301965.9:n.*416G>T
ENST00000436784.6:c.1297G>T	ENSP00000389175.2:p.Glu433Ter
ENST00000461183.5:c.764-195G>T	ENSP00000417264.1:n.764-195G>T
ENST00000471180.5:c.635-195G>T	ENSP00000417526.1:n.635-195G>T
ENST00000473032.5:c.530-195G>T	ENSP00000418951.1:n.530-195G>T
ENST00000477382.1:c.*416G>T	ENSP00000419008.1:n.*416G>T
ENST00000486393.5:c.*660G>T	ENSP00000419868.1:n.*660G>T
ENST00000489173.1:n.1591G>T
NM_001144951.1:c.*416G>T	NP_001138423.1:n.*416G>T
NM_145262.3:c.1297G>T	NP_660305.2:p.Glu433Ter
NR_026699.1:n.1395G>T
NR_026700.1:n.696-195G>T
NR_026701.1:n.1393G>T
NR_026702.1:n.626-195G>T
XM_005264878.2:c.*416G>T	XP_005264935.1:n.*416G>T
XR_245095.2:n.2743-195G>T
XM_017005730.1:c.916G>T	XP_016861219.1:p.Glu306Ter
XM_024453351.1:c.1297G>T	XP_024309119.1:p.Glu433Ter
XM_024453352.1:c.*416G>T	XP_024309120.1:n.*416G>T
XR_001740022.2:n.3199G>T
XR_001740023.2:n.2918-195G>T
XR_245095.4:n.2744-195G>T
NM_145262.4:c.1297G>T MANE Select	NP_660305.2:p.Glu433Ter
NR_026699.2:n.1387G>T
NR_026700.2:n.688-195G>T
NR_026701.2:n.1385G>T
NR_026702.2:n.618-195G>T
NM_001144951.2:c.*416G>T	NP_001138423.1:n.*416G>T