Canonical Allele Identifier: CA1364789363

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1578032792

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293297T>C , CM000665.2:g.52293297T>C	GRCh38
NC_000003.11:g.52327313T>C , CM000665.1:g.52327313T>C	GRCh37
NC_000003.10:g.52302353T>C	NCBI36
NG_023246.1:g.10478T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*171T>C MANE Select	ENSP00000389175.2:n.*171T>C
ENST00000436784.6:c.*171T>C	ENSP00000389175.2:n.*171T>C
ENST00000471180.5:c.*59-10T>C	ENSP00000417526.1:n.*59-10T>C
ENST00000473032.5:c.*59-10T>C	ENSP00000418951.1:n.*59-10T>C
ENST00000486393.5:c.*1106T>C	ENSP00000419868.1:n.*1106T>C
ENST00000489173.1:n.1915-10T>C
NM_145262.3:c.*171T>C	NP_660305.2:n.*171T>C
NR_026699.1:n.1841T>C
NR_026700.1:n.843-10T>C
NR_026701.1:n.1735-10T>C
NR_026702.1:n.773-10T>C
XM_005264878.2:c.*862T>C	XP_005264935.1:n.*862T>C
XR_245095.2:n.2890-10T>C
XM_017005730.1:c.*171T>C	XP_016861219.1:n.*171T>C
XM_024453351.1:c.*171T>C	XP_024309119.1:n.*171T>C
XM_024453352.1:c.*862T>C	XP_024309120.1:n.*862T>C
XR_001740022.2:n.3541-10T>C
XR_001740023.2:n.3065-10T>C
XR_245095.4:n.2891-10T>C
NM_145262.4:c.*171T>C MANE Select	NP_660305.2:n.*171T>C
NR_026699.2:n.1833T>C
NR_026700.2:n.835-10T>C
NR_026701.2:n.1727-10T>C
NR_026702.2:n.765-10T>C
NM_001144951.2:c.*862T>C	NP_001138423.1:n.*862T>C