Canonical Allele Identifier: CA353076875

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327127C>G (hg19) ; chr3:g.52293111C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293111C>G , CM000665.2:g.52293111C>G	GRCh38
NC_000003.11:g.52327127C>G , CM000665.1:g.52327127C>G	GRCh37
NC_000003.10:g.52302167C>G	NCBI36
NG_023246.1:g.10292C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1557C>G MANE Select	ENSP00000389175.2:p.Phe519Leu
ENST00000436784.6:c.1557C>G	ENSP00000389175.2:p.Phe519Leu
ENST00000461183.5:c.829C>G	ENSP00000417264.1:p.Pro277Ala
ENST00000471180.5:c.700C>G	ENSP00000417526.1:p.Pro234Ala
ENST00000473032.5:c.595C>G	ENSP00000418951.1:p.Pro199Ala
ENST00000486393.5:c.*920C>G	ENSP00000419868.1:n.*920C>G
ENST00000489173.1:n.1851C>G
NM_145262.3:c.1557C>G	NP_660305.2:p.Phe519Leu
NR_026699.1:n.1655C>G
NR_026700.1:n.761C>G
NR_026701.1:n.1653C>G
NR_026702.1:n.691C>G
XM_005264878.2:c.*676C>G	XP_005264935.1:n.*676C>G
XR_245095.2:n.2808C>G
XM_017005730.1:c.1176C>G	XP_016861219.1:p.Phe392Leu
XM_024453351.1:c.1557C>G	XP_024309119.1:p.Phe519Leu
XM_024453352.1:c.*676C>G	XP_024309120.1:n.*676C>G
XR_001740022.2:n.3459C>G
XR_001740023.2:n.2983C>G
XR_245095.4:n.2809C>G
NM_145262.4:c.1557C>G MANE Select	NP_660305.2:p.Phe519Leu
NR_026699.2:n.1647C>G
NR_026700.2:n.753C>G
NR_026701.2:n.1645C>G
NR_026702.2:n.683C>G
NM_001144951.2:c.*676C>G	NP_001138423.1:n.*676C>G