Canonical Allele Identifier: CA2432029

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52290667G>A , CM000665.2:g.52290667G>A	GRCh38
NC_000003.11:g.52324683G>A , CM000665.1:g.52324683G>A	GRCh37
NC_000003.10:g.52299723G>A	NCBI36
NG_023246.1:g.7848G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_145262.4:c.325G>A MANE Select	NP_660305.2:p.Val109Met
ENST00000436784.7:c.325G>A MANE Select	ENSP00000389175.2:p.Val109Met
NM_001144951.1:c.325G>A	NP_001138423.1:p.Val109Met
NM_001144951.2:c.325G>A	NP_001138423.1:p.Val109Met
NM_145262.3:c.325G>A	NP_660305.2:p.Val109Met
NR_026699.1:n.421G>A
NR_026699.2:n.413G>A
NR_026700.1:n.58-293G>A
NR_026700.2:n.50-293G>A
NR_026701.1:n.421G>A
NR_026701.2:n.413G>A
NR_026702.1:n.421G>A
NR_026702.2:n.413G>A
ENST00000305690.12:c.325G>A	ENSP00000301965.9:p.Val109Met
ENST00000436784.6:c.325G>A	ENSP00000389175.2:p.Val109Met
ENST00000461183.5:c.126-293G>A	ENSP00000417264.1:n.126-293G>A
ENST00000471180.5:c.-4-293G>A	ENSP00000417526.1:n.-4-293G>A
ENST00000473032.5:c.325G>A	ENSP00000418951.1:p.Val109Met
ENST00000473583.1:n.594G>A
ENST00000477382.1:c.325G>A	ENSP00000419008.1:p.Val109Met
ENST00000486393.5:c.325G>A	ENSP00000419868.1:p.Val109Met
XM_005264878.2:c.325G>A	XP_005264935.1:p.Val109Met
XM_017005730.1:c.-4-293G>A	XP_016861219.1:n.-4-293G>A
XM_024453351.1:c.325G>A	XP_024309119.1:p.Val109Met
XM_024453352.1:c.325G>A	XP_024309120.1:p.Val109Met
XR_001740022.2:n.2227G>A
XR_001740023.2:n.2227G>A
XR_245095.2:n.2228G>A
XR_245095.4:n.2229G>A