Canonical Allele Identifier: CA908119849

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1270267168
• MyVariant Identifiers: chr3:g.52327288C>T (hg19) ; chr3:g.52293272C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293272C>T , CM000665.2:g.52293272C>T	GRCh38
NC_000003.11:g.52327288C>T , CM000665.1:g.52327288C>T	GRCh37
NC_000003.10:g.52302328C>T	NCBI36
NG_023246.1:g.10453C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*146C>T MANE Select	ENSP00000389175.2:n.*146C>T
ENST00000436784.6:c.*146C>T	ENSP00000389175.2:n.*146C>T
ENST00000471180.5:c.*59-35C>T	ENSP00000417526.1:n.*59-35C>T
ENST00000473032.5:c.*59-35C>T	ENSP00000418951.1:n.*59-35C>T
ENST00000486393.5:c.*1081C>T	ENSP00000419868.1:n.*1081C>T
ENST00000489173.1:n.1915-35C>T
NM_145262.3:c.*146C>T	NP_660305.2:n.*146C>T
NR_026699.1:n.1816C>T
NR_026700.1:n.843-35C>T
NR_026701.1:n.1735-35C>T
NR_026702.1:n.773-35C>T
XM_005264878.2:c.*837C>T	XP_005264935.1:n.*837C>T
XR_245095.2:n.2890-35C>T
XM_017005730.1:c.*146C>T	XP_016861219.1:n.*146C>T
XM_024453351.1:c.*146C>T	XP_024309119.1:n.*146C>T
XM_024453352.1:c.*837C>T	XP_024309120.1:n.*837C>T
XR_001740022.2:n.3541-35C>T
XR_001740023.2:n.3065-35C>T
XR_245095.4:n.2891-35C>T
NM_145262.4:c.*146C>T MANE Select	NP_660305.2:n.*146C>T
NR_026699.2:n.1808C>T
NR_026700.2:n.835-35C>T
NR_026701.2:n.1727-35C>T
NR_026702.2:n.765-35C>T
NM_001144951.2:c.*837C>T	NP_001138423.1:n.*837C>T