Canonical Allele Identifier: CA353076608

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327075T>C (hg19) ; chr3:g.52293059T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293059T>C , CM000665.2:g.52293059T>C	GRCh38
NC_000003.11:g.52327075T>C , CM000665.1:g.52327075T>C	GRCh37
NC_000003.10:g.52302115T>C	NCBI36
NG_023246.1:g.10240T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1505T>C MANE Select	ENSP00000389175.2:p.Leu502Pro
ENST00000436784.6:c.1505T>C	ENSP00000389175.2:p.Leu502Pro
ENST00000461183.5:c.777T>C	ENSP00000417264.1:p.Pro259=
ENST00000471180.5:c.648T>C	ENSP00000417526.1:p.Pro216=
ENST00000473032.5:c.543T>C	ENSP00000418951.1:p.Pro181=
ENST00000486393.5:c.*868T>C	ENSP00000419868.1:n.*868T>C
ENST00000489173.1:n.1799T>C
NM_145262.3:c.1505T>C	NP_660305.2:p.Leu502Pro
NR_026699.1:n.1603T>C
NR_026700.1:n.709T>C
NR_026701.1:n.1601T>C
NR_026702.1:n.639T>C
XM_005264878.2:c.*624T>C	XP_005264935.1:n.*624T>C
XR_245095.2:n.2756T>C
XM_017005730.1:c.1124T>C	XP_016861219.1:p.Leu375Pro
XM_024453351.1:c.1505T>C	XP_024309119.1:p.Leu502Pro
XM_024453352.1:c.*624T>C	XP_024309120.1:n.*624T>C
XR_001740022.2:n.3407T>C
XR_001740023.2:n.2931T>C
XR_245095.4:n.2757T>C
NM_145262.4:c.1505T>C MANE Select	NP_660305.2:p.Leu502Pro
NR_026699.2:n.1595T>C
NR_026700.2:n.701T>C
NR_026701.2:n.1593T>C
NR_026702.2:n.631T>C
NM_001144951.2:c.*624T>C	NP_001138423.1:n.*624T>C