Canonical Allele Identifier: CA353076756

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327107A>C (hg19) ; chr3:g.52293091A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293091A>C , CM000665.2:g.52293091A>C	GRCh38
NC_000003.11:g.52327107A>C , CM000665.1:g.52327107A>C	GRCh37
NC_000003.10:g.52302147A>C	NCBI36
NG_023246.1:g.10272A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1537A>C MANE Select	ENSP00000389175.2:p.Met513Leu
ENST00000436784.6:c.1537A>C	ENSP00000389175.2:p.Met513Leu
ENST00000461183.5:c.809A>C	ENSP00000417264.1:p.His270Pro
ENST00000471180.5:c.680A>C	ENSP00000417526.1:p.His227Pro
ENST00000473032.5:c.575A>C	ENSP00000418951.1:p.His192Pro
ENST00000486393.5:c.*900A>C	ENSP00000419868.1:n.*900A>C
ENST00000489173.1:n.1831A>C
NM_145262.3:c.1537A>C	NP_660305.2:p.Met513Leu
NR_026699.1:n.1635A>C
NR_026700.1:n.741A>C
NR_026701.1:n.1633A>C
NR_026702.1:n.671A>C
XM_005264878.2:c.*656A>C	XP_005264935.1:n.*656A>C
XR_245095.2:n.2788A>C
XM_017005730.1:c.1156A>C	XP_016861219.1:p.Met386Leu
XM_024453351.1:c.1537A>C	XP_024309119.1:p.Met513Leu
XM_024453352.1:c.*656A>C	XP_024309120.1:n.*656A>C
XR_001740022.2:n.3439A>C
XR_001740023.2:n.2963A>C
XR_245095.4:n.2789A>C
NM_145262.4:c.1537A>C MANE Select	NP_660305.2:p.Met513Leu
NR_026699.2:n.1627A>C
NR_026700.2:n.733A>C
NR_026701.2:n.1625A>C
NR_026702.2:n.663A>C
NM_001144951.2:c.*656A>C	NP_001138423.1:n.*656A>C