Canonical Allele Identifier: CA353076556

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327064T>C (hg19) ; chr3:g.52293048T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293048T>C , CM000665.2:g.52293048T>C	GRCh38
NC_000003.11:g.52327064T>C , CM000665.1:g.52327064T>C	GRCh37
NC_000003.10:g.52302104T>C	NCBI36
NG_023246.1:g.10229T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1494T>C MANE Select	ENSP00000389175.2:p.Gly498=
ENST00000436784.6:c.1494T>C	ENSP00000389175.2:p.Gly498=
ENST00000461183.5:c.766T>C	ENSP00000417264.1:p.Trp256Arg
ENST00000471180.5:c.637T>C	ENSP00000417526.1:p.Trp213Arg
ENST00000473032.5:c.532T>C	ENSP00000418951.1:p.Trp178Arg
ENST00000486393.5:c.*857T>C	ENSP00000419868.1:n.*857T>C
ENST00000489173.1:n.1788T>C
NM_145262.3:c.1494T>C	NP_660305.2:p.Gly498=
NR_026699.1:n.1592T>C
NR_026700.1:n.698T>C
NR_026701.1:n.1590T>C
NR_026702.1:n.628T>C
XM_005264878.2:c.*613T>C	XP_005264935.1:n.*613T>C
XR_245095.2:n.2745T>C
XM_017005730.1:c.1113T>C	XP_016861219.1:p.Gly371=
XM_024453351.1:c.1494T>C	XP_024309119.1:p.Gly498=
XM_024453352.1:c.*613T>C	XP_024309120.1:n.*613T>C
XR_001740022.2:n.3396T>C
XR_001740023.2:n.2920T>C
XR_245095.4:n.2746T>C
NM_145262.4:c.1494T>C MANE Select	NP_660305.2:p.Gly498=
NR_026699.2:n.1584T>C
NR_026700.2:n.690T>C
NR_026701.2:n.1582T>C
NR_026702.2:n.620T>C
NM_001144951.2:c.*613T>C	NP_001138423.1:n.*613T>C