Canonical Allele Identifier: CA353076209

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1316561468
• gnomAD v2: 3-52326991-C-T
• gnomAD v4: 3-52292975-C-T
• MyVariant Identifiers: chr3:g.52326991C>T (hg19) ; chr3:g.52292975C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292975C>T , CM000665.2:g.52292975C>T	GRCh38
NC_000003.11:g.52326991C>T , CM000665.1:g.52326991C>T	GRCh37
NC_000003.10:g.52302031C>T	NCBI36
NG_023246.1:g.10156C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1421C>T MANE Select	ENSP00000389175.2:p.Ala474Val
ENST00000305690.12:c.*540C>T	ENSP00000301965.9:n.*540C>T
ENST00000436784.6:c.1421C>T	ENSP00000389175.2:p.Ala474Val
ENST00000461183.5:c.764-71C>T	ENSP00000417264.1:n.764-71C>T
ENST00000471180.5:c.635-71C>T	ENSP00000417526.1:n.635-71C>T
ENST00000473032.5:c.530-71C>T	ENSP00000418951.1:n.530-71C>T
ENST00000477382.1:c.*540C>T	ENSP00000419008.1:n.*540C>T
ENST00000486393.5:c.*784C>T	ENSP00000419868.1:n.*784C>T
ENST00000489173.1:n.1715C>T
NM_001144951.1:c.*540C>T	NP_001138423.1:n.*540C>T
NM_145262.3:c.1421C>T	NP_660305.2:p.Ala474Val
NR_026699.1:n.1519C>T
NR_026700.1:n.696-71C>T
NR_026701.1:n.1517C>T
NR_026702.1:n.626-71C>T
XM_005264878.2:c.*540C>T	XP_005264935.1:n.*540C>T
XR_245095.2:n.2743-71C>T
XM_017005730.1:c.1040C>T	XP_016861219.1:p.Ala347Val
XM_024453351.1:c.1421C>T	XP_024309119.1:p.Ala474Val
XM_024453352.1:c.*540C>T	XP_024309120.1:n.*540C>T
XR_001740022.2:n.3323C>T
XR_001740023.2:n.2918-71C>T
XR_245095.4:n.2744-71C>T
NM_145262.4:c.1421C>T MANE Select	NP_660305.2:p.Ala474Val
NR_026699.2:n.1511C>T
NR_026700.2:n.688-71C>T
NR_026701.2:n.1509C>T
NR_026702.2:n.618-71C>T
NM_001144951.2:c.*540C>T	NP_001138423.1:n.*540C>T