Canonical Allele Identifier: CA353076976

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1700539865
• gnomAD v4: 3-52293129-G-A
• MyVariant Identifiers: chr3:g.52327145G>A (hg19) ; chr3:g.52293129G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293129G>A , CM000665.2:g.52293129G>A	GRCh38
NC_000003.11:g.52327145G>A , CM000665.1:g.52327145G>A	GRCh37
NC_000003.10:g.52302185G>A	NCBI36
NG_023246.1:g.10310G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.*3G>A MANE Select	ENSP00000389175.2:n.*3G>A
ENST00000436784.6:c.*3G>A	ENSP00000389175.2:n.*3G>A
ENST00000461183.5:c.847G>A	ENSP00000417264.1:p.Ala283Thr
ENST00000471180.5:c.718G>A	ENSP00000417526.1:p.Ala240Thr
ENST00000473032.5:c.613G>A	ENSP00000418951.1:p.Ala205Thr
ENST00000486393.5:c.*938G>A	ENSP00000419868.1:n.*938G>A
ENST00000489173.1:n.1869G>A
NM_145262.3:c.*3G>A	NP_660305.2:n.*3G>A
NR_026699.1:n.1673G>A
NR_026700.1:n.779G>A
NR_026701.1:n.1671G>A
NR_026702.1:n.709G>A
XM_005264878.2:c.*694G>A	XP_005264935.1:n.*694G>A
XR_245095.2:n.2826G>A
XM_017005730.1:c.*3G>A	XP_016861219.1:n.*3G>A
XM_024453351.1:c.*3G>A	XP_024309119.1:n.*3G>A
XM_024453352.1:c.*694G>A	XP_024309120.1:n.*694G>A
XR_001740022.2:n.3477G>A
XR_001740023.2:n.3001G>A
XR_245095.4:n.2827G>A
NM_145262.4:c.*3G>A MANE Select	NP_660305.2:n.*3G>A
NR_026699.2:n.1665G>A
NR_026700.2:n.771G>A
NR_026701.2:n.1663G>A
NR_026702.2:n.701G>A
NM_001144951.2:c.*694G>A	NP_001138423.1:n.*694G>A