Canonical Allele Identifier: CA353076829

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327120T>C (hg19) ; chr3:g.52293104T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293104T>C , CM000665.2:g.52293104T>C	GRCh38
NC_000003.11:g.52327120T>C , CM000665.1:g.52327120T>C	GRCh37
NC_000003.10:g.52302160T>C	NCBI36
NG_023246.1:g.10285T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1550T>C MANE Select	ENSP00000389175.2:p.Leu517Pro
ENST00000436784.6:c.1550T>C	ENSP00000389175.2:p.Leu517Pro
ENST00000461183.5:c.822T>C	ENSP00000417264.1:p.Pro274=
ENST00000471180.5:c.693T>C	ENSP00000417526.1:p.Pro231=
ENST00000473032.5:c.588T>C	ENSP00000418951.1:p.Pro196=
ENST00000486393.5:c.*913T>C	ENSP00000419868.1:n.*913T>C
ENST00000489173.1:n.1844T>C
NM_145262.3:c.1550T>C	NP_660305.2:p.Leu517Pro
NR_026699.1:n.1648T>C
NR_026700.1:n.754T>C
NR_026701.1:n.1646T>C
NR_026702.1:n.684T>C
XM_005264878.2:c.*669T>C	XP_005264935.1:n.*669T>C
XR_245095.2:n.2801T>C
XM_017005730.1:c.1169T>C	XP_016861219.1:p.Leu390Pro
XM_024453351.1:c.1550T>C	XP_024309119.1:p.Leu517Pro
XM_024453352.1:c.*669T>C	XP_024309120.1:n.*669T>C
XR_001740022.2:n.3452T>C
XR_001740023.2:n.2976T>C
XR_245095.4:n.2802T>C
NM_145262.4:c.1550T>C MANE Select	NP_660305.2:p.Leu517Pro
NR_026699.2:n.1640T>C
NR_026700.2:n.746T>C
NR_026701.2:n.1638T>C
NR_026702.2:n.676T>C
NM_001144951.2:c.*669T>C	NP_001138423.1:n.*669T>C