Canonical Allele Identifier: CA543056251

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1363739067
• gnomAD v2: 3-52327299-T-C
• gnomAD v3: 3-52293283-T-C
• gnomAD v4: 3-52293283-T-C
• MyVariant Identifiers: chr3:g.52327299T>C (hg19) ; chr3:g.52293283T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293283T>C , CM000665.2:g.52293283T>C	GRCh38
NC_000003.11:g.52327299T>C , CM000665.1:g.52327299T>C	GRCh37
NC_000003.10:g.52302339T>C	NCBI36
NG_023246.1:g.10464T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*157T>C MANE Select	ENSP00000389175.2:n.*157T>C
ENST00000436784.6:c.*157T>C	ENSP00000389175.2:n.*157T>C
ENST00000471180.5:c.*59-24T>C	ENSP00000417526.1:n.*59-24T>C
ENST00000473032.5:c.*59-24T>C	ENSP00000418951.1:n.*59-24T>C
ENST00000486393.5:c.*1092T>C	ENSP00000419868.1:n.*1092T>C
ENST00000489173.1:n.1915-24T>C
NM_145262.3:c.*157T>C	NP_660305.2:n.*157T>C
NR_026699.1:n.1827T>C
NR_026700.1:n.843-24T>C
NR_026701.1:n.1735-24T>C
NR_026702.1:n.773-24T>C
XM_005264878.2:c.*848T>C	XP_005264935.1:n.*848T>C
XR_245095.2:n.2890-24T>C
XM_017005730.1:c.*157T>C	XP_016861219.1:n.*157T>C
XM_024453351.1:c.*157T>C	XP_024309119.1:n.*157T>C
XM_024453352.1:c.*848T>C	XP_024309120.1:n.*848T>C
XR_001740022.2:n.3541-24T>C
XR_001740023.2:n.3065-24T>C
XR_245095.4:n.2891-24T>C
NM_145262.4:c.*157T>C MANE Select	NP_660305.2:n.*157T>C
NR_026699.2:n.1819T>C
NR_026700.2:n.835-24T>C
NR_026701.2:n.1727-24T>C
NR_026702.2:n.765-24T>C
NM_001144951.2:c.*848T>C	NP_001138423.1:n.*848T>C