Canonical Allele Identifier: CA353074901

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52292620-A-G
• MyVariant Identifiers: chr3:g.52326636A>G (hg19) ; chr3:g.52292620A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292620A>G , CM000665.2:g.52292620A>G	GRCh38
NC_000003.11:g.52326636A>G , CM000665.1:g.52326636A>G	GRCh37
NC_000003.10:g.52301676A>G	NCBI36
NG_023246.1:g.9801A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1066A>G MANE Select	ENSP00000389175.2:p.Arg356Gly
ENST00000305690.12:c.*185A>G	ENSP00000301965.9:n.*185A>G
ENST00000436784.6:c.1066A>G	ENSP00000389175.2:p.Arg356Gly
ENST00000461183.5:c.763+51A>G	ENSP00000417264.1:n.763+51A>G
ENST00000471180.5:c.634+51A>G	ENSP00000417526.1:n.634+51A>G
ENST00000473032.5:c.530-426A>G	ENSP00000418951.1:n.530-426A>G
ENST00000477382.1:c.*185A>G	ENSP00000419008.1:n.*185A>G
ENST00000486393.5:c.*429A>G	ENSP00000419868.1:n.*429A>G
ENST00000489173.1:n.1360A>G
NM_001144951.1:c.*185A>G	NP_001138423.1:n.*185A>G
NM_145262.3:c.1066A>G	NP_660305.2:p.Arg356Gly
NR_026699.1:n.1164A>G
NR_026700.1:n.695+51A>G
NR_026701.1:n.1162A>G
NR_026702.1:n.626-426A>G
XM_005264878.2:c.*185A>G	XP_005264935.1:n.*185A>G
XR_245095.2:n.2742+51A>G
XM_017005730.1:c.685A>G	XP_016861219.1:p.Arg229Gly
XM_024453351.1:c.1066A>G	XP_024309119.1:p.Arg356Gly
XM_024453352.1:c.*185A>G	XP_024309120.1:n.*185A>G
XR_001740022.2:n.2968A>G
XR_001740023.2:n.2917+51A>G
XR_245095.4:n.2743+51A>G
NM_145262.4:c.1066A>G MANE Select	NP_660305.2:p.Arg356Gly
NR_026699.2:n.1156A>G
NR_026700.2:n.687+51A>G
NR_026701.2:n.1154A>G
NR_026702.2:n.618-426A>G
NM_001144951.2:c.*185A>G	NP_001138423.1:n.*185A>G