Canonical Allele Identifier: CA353075499

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1289039172
• MyVariant Identifiers: chr3:g.52326783C>G (hg19) ; chr3:g.52292767C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292767C>G , CM000665.2:g.52292767C>G	GRCh38
NC_000003.11:g.52326783C>G , CM000665.1:g.52326783C>G	GRCh37
NC_000003.10:g.52301823C>G	NCBI36
NG_023246.1:g.9948C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1213C>G MANE Select	ENSP00000389175.2:p.Leu405Val
ENST00000305690.12:c.*332C>G	ENSP00000301965.9:n.*332C>G
ENST00000436784.6:c.1213C>G	ENSP00000389175.2:p.Leu405Val
ENST00000461183.5:c.763+198C>G	ENSP00000417264.1:n.763+198C>G
ENST00000471180.5:c.634+198C>G	ENSP00000417526.1:n.634+198C>G
ENST00000473032.5:c.530-279C>G	ENSP00000418951.1:n.530-279C>G
ENST00000477382.1:c.*332C>G	ENSP00000419008.1:n.*332C>G
ENST00000486393.5:c.*576C>G	ENSP00000419868.1:n.*576C>G
ENST00000489173.1:n.1507C>G
NM_001144951.1:c.*332C>G	NP_001138423.1:n.*332C>G
NM_145262.3:c.1213C>G	NP_660305.2:p.Leu405Val
NR_026699.1:n.1311C>G
NR_026700.1:n.695+198C>G
NR_026701.1:n.1309C>G
NR_026702.1:n.626-279C>G
XM_005264878.2:c.*332C>G	XP_005264935.1:n.*332C>G
XR_245095.2:n.2742+198C>G
XM_017005730.1:c.832C>G	XP_016861219.1:p.Leu278Val
XM_024453351.1:c.1213C>G	XP_024309119.1:p.Leu405Val
XM_024453352.1:c.*332C>G	XP_024309120.1:n.*332C>G
XR_001740022.2:n.3115C>G
XR_001740023.2:n.2917+198C>G
XR_245095.4:n.2743+198C>G
NM_145262.4:c.1213C>G MANE Select	NP_660305.2:p.Leu405Val
NR_026699.2:n.1303C>G
NR_026700.2:n.687+198C>G
NR_026701.2:n.1301C>G
NR_026702.2:n.618-279C>G
NM_001144951.2:c.*332C>G	NP_001138423.1:n.*332C>G