Canonical Allele Identifier: CA74736939

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1023916136
• gnomAD v2: 3-52327256-G-A
• gnomAD v3: 3-52293240-G-A
• gnomAD v4: 3-52293240-G-A
• MyVariant Identifiers: chr3:g.52327256G>A (hg19) ; chr3:g.52293240G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293240G>A , CM000665.2:g.52293240G>A	GRCh38
NC_000003.11:g.52327256G>A , CM000665.1:g.52327256G>A	GRCh37
NC_000003.10:g.52302296G>A	NCBI36
NG_023246.1:g.10421G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*114G>A MANE Select	ENSP00000389175.2:n.*114G>A
ENST00000436784.6:c.*114G>A	ENSP00000389175.2:n.*114G>A
ENST00000471180.5:c.*58+48G>A	ENSP00000417526.1:n.*58+48G>A
ENST00000473032.5:c.*58+48G>A	ENSP00000418951.1:n.*58+48G>A
ENST00000486393.5:c.*1049G>A	ENSP00000419868.1:n.*1049G>A
ENST00000489173.1:n.1915-67G>A
NM_145262.3:c.*114G>A	NP_660305.2:n.*114G>A
NR_026699.1:n.1784G>A
NR_026700.1:n.842+48G>A
NR_026701.1:n.1734+48G>A
NR_026702.1:n.772+48G>A
XM_005264878.2:c.*805G>A	XP_005264935.1:n.*805G>A
XR_245095.2:n.2889+48G>A
XM_017005730.1:c.*114G>A	XP_016861219.1:n.*114G>A
XM_024453351.1:c.*114G>A	XP_024309119.1:n.*114G>A
XM_024453352.1:c.*805G>A	XP_024309120.1:n.*805G>A
XR_001740022.2:n.3540+48G>A
XR_001740023.2:n.3064+48G>A
XR_245095.4:n.2890+48G>A
NM_145262.4:c.*114G>A MANE Select	NP_660305.2:n.*114G>A
NR_026699.2:n.1776G>A
NR_026700.2:n.834+48G>A
NR_026701.2:n.1726+48G>A
NR_026702.2:n.764+48G>A
NM_001144951.2:c.*805G>A	NP_001138423.1:n.*805G>A