Canonical Allele Identifier: CA353076936

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327138G>C (hg19) ; chr3:g.52293122G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293122G>C , CM000665.2:g.52293122G>C	GRCh38
NC_000003.11:g.52327138G>C , CM000665.1:g.52327138G>C	GRCh37
NC_000003.10:g.52302178G>C	NCBI36
NG_023246.1:g.10303G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1568G>C MANE Select	ENSP00000389175.2:p.Arg523Pro
ENST00000436784.6:c.1568G>C	ENSP00000389175.2:p.Arg523Pro
ENST00000461183.5:c.840G>C	ENSP00000417264.1:p.Ser280=
ENST00000471180.5:c.711G>C	ENSP00000417526.1:p.Ser237=
ENST00000473032.5:c.606G>C	ENSP00000418951.1:p.Ser202=
ENST00000486393.5:c.*931G>C	ENSP00000419868.1:n.*931G>C
ENST00000489173.1:n.1862G>C
NM_145262.3:c.1568G>C	NP_660305.2:p.Arg523Pro
NR_026699.1:n.1666G>C
NR_026700.1:n.772G>C
NR_026701.1:n.1664G>C
NR_026702.1:n.702G>C
XM_005264878.2:c.*687G>C	XP_005264935.1:n.*687G>C
XR_245095.2:n.2819G>C
XM_017005730.1:c.1187G>C	XP_016861219.1:p.Arg396Pro
XM_024453351.1:c.1568G>C	XP_024309119.1:p.Arg523Pro
XM_024453352.1:c.*687G>C	XP_024309120.1:n.*687G>C
XR_001740022.2:n.3470G>C
XR_001740023.2:n.2994G>C
XR_245095.4:n.2820G>C
NM_145262.4:c.1568G>C MANE Select	NP_660305.2:p.Arg523Pro
NR_026699.2:n.1658G>C
NR_026700.2:n.764G>C
NR_026701.2:n.1656G>C
NR_026702.2:n.694G>C
NM_001144951.2:c.*687G>C	NP_001138423.1:n.*687G>C