Canonical Allele Identifier: CA353075508

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1438274165
• gnomAD v2: 3-52326789-G-A
• gnomAD v4: 3-52292773-G-A
• MyVariant Identifiers: chr3:g.52326789G>A (hg19) ; chr3:g.52292773G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292773G>A , CM000665.2:g.52292773G>A	GRCh38
NC_000003.11:g.52326789G>A , CM000665.1:g.52326789G>A	GRCh37
NC_000003.10:g.52301829G>A	NCBI36
NG_023246.1:g.9954G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1219G>A MANE Select	ENSP00000389175.2:p.Gly407Ser
ENST00000305690.12:c.*338G>A	ENSP00000301965.9:n.*338G>A
ENST00000436784.6:c.1219G>A	ENSP00000389175.2:p.Gly407Ser
ENST00000461183.5:c.763+204G>A	ENSP00000417264.1:n.763+204G>A
ENST00000471180.5:c.634+204G>A	ENSP00000417526.1:n.634+204G>A
ENST00000473032.5:c.530-273G>A	ENSP00000418951.1:n.530-273G>A
ENST00000477382.1:c.*338G>A	ENSP00000419008.1:n.*338G>A
ENST00000486393.5:c.*582G>A	ENSP00000419868.1:n.*582G>A
ENST00000489173.1:n.1513G>A
NM_001144951.1:c.*338G>A	NP_001138423.1:n.*338G>A
NM_145262.3:c.1219G>A	NP_660305.2:p.Gly407Ser
NR_026699.1:n.1317G>A
NR_026700.1:n.695+204G>A
NR_026701.1:n.1315G>A
NR_026702.1:n.626-273G>A
XM_005264878.2:c.*338G>A	XP_005264935.1:n.*338G>A
XR_245095.2:n.2742+204G>A
XM_017005730.1:c.838G>A	XP_016861219.1:p.Gly280Ser
XM_024453351.1:c.1219G>A	XP_024309119.1:p.Gly407Ser
XM_024453352.1:c.*338G>A	XP_024309120.1:n.*338G>A
XR_001740022.2:n.3121G>A
XR_001740023.2:n.2917+204G>A
XR_245095.4:n.2743+204G>A
NM_145262.4:c.1219G>A MANE Select	NP_660305.2:p.Gly407Ser
NR_026699.2:n.1309G>A
NR_026700.2:n.687+204G>A
NR_026701.2:n.1307G>A
NR_026702.2:n.618-273G>A
NM_001144951.2:c.*338G>A	NP_001138423.1:n.*338G>A