Canonical Allele Identifier: CA353076241

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326999G>T (hg19) ; chr3:g.52292983G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292983G>T , CM000665.2:g.52292983G>T	GRCh38
NC_000003.11:g.52326999G>T , CM000665.1:g.52326999G>T	GRCh37
NC_000003.10:g.52302039G>T	NCBI36
NG_023246.1:g.10164G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1429G>T MANE Select	ENSP00000389175.2:p.Gly477Cys
ENST00000305690.12:c.*548G>T	ENSP00000301965.9:n.*548G>T
ENST00000436784.6:c.1429G>T	ENSP00000389175.2:p.Gly477Cys
ENST00000461183.5:c.764-63G>T	ENSP00000417264.1:n.764-63G>T
ENST00000471180.5:c.635-63G>T	ENSP00000417526.1:n.635-63G>T
ENST00000473032.5:c.530-63G>T	ENSP00000418951.1:n.530-63G>T
ENST00000477382.1:c.*548G>T	ENSP00000419008.1:n.*548G>T
ENST00000486393.5:c.*792G>T	ENSP00000419868.1:n.*792G>T
ENST00000489173.1:n.1723G>T
NM_001144951.1:c.*548G>T	NP_001138423.1:n.*548G>T
NM_145262.3:c.1429G>T	NP_660305.2:p.Gly477Cys
NR_026699.1:n.1527G>T
NR_026700.1:n.696-63G>T
NR_026701.1:n.1525G>T
NR_026702.1:n.626-63G>T
XM_005264878.2:c.*548G>T	XP_005264935.1:n.*548G>T
XR_245095.2:n.2743-63G>T
XM_017005730.1:c.1048G>T	XP_016861219.1:p.Gly350Cys
XM_024453351.1:c.1429G>T	XP_024309119.1:p.Gly477Cys
XM_024453352.1:c.*548G>T	XP_024309120.1:n.*548G>T
XR_001740022.2:n.3331G>T
XR_001740023.2:n.2918-63G>T
XR_245095.4:n.2744-63G>T
NM_145262.4:c.1429G>T MANE Select	NP_660305.2:p.Gly477Cys
NR_026699.2:n.1519G>T
NR_026700.2:n.688-63G>T
NR_026701.2:n.1517G>T
NR_026702.2:n.618-63G>T
NM_001144951.2:c.*548G>T	NP_001138423.1:n.*548G>T