Canonical Allele Identifier: CA2573137260

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52291733C>A , CM000665.2:g.52291733C>A	GRCh38
NC_000003.11:g.52325749C>A , CM000665.1:g.52325749C>A	GRCh37
NC_000003.10:g.52300789C>A	NCBI36
NG_023246.1:g.8914C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_145262.4:c.530-14C>A MANE Select	NP_660305.2:n.530-14C>A
ENST00000436784.7:c.530-14C>A MANE Select	ENSP00000389175.2:n.530-14C>A
NM_001144951.1:c.530-527C>A	NP_001138423.1:n.530-527C>A
NM_001144951.2:c.530-527C>A	NP_001138423.1:n.530-527C>A
NM_145262.3:c.530-14C>A	NP_660305.2:n.530-14C>A
NR_026699.1:n.626-12C>A
NR_026699.2:n.618-12C>A
NR_026700.1:n.210-14C>A
NR_026700.2:n.202-14C>A
NR_026701.1:n.626-14C>A
NR_026701.2:n.618-14C>A
NR_026702.1:n.625+622C>A
NR_026702.2:n.617+622C>A
ENST00000305690.12:c.530-527C>A	ENSP00000301965.9:n.530-527C>A
ENST00000436784.6:c.530-14C>A	ENSP00000389175.2:n.530-14C>A
ENST00000461183.5:c.278-14C>A	ENSP00000417264.1:n.278-14C>A
ENST00000471180.5:c.149-14C>A	ENSP00000417526.1:n.149-14C>A
ENST00000473032.5:c.529+622C>A	ENSP00000418951.1:n.529+622C>A
ENST00000473583.1:n.799-527C>A
ENST00000477382.1:c.530-527C>A	ENSP00000419008.1:n.530-527C>A
ENST00000486393.5:c.530-12C>A	ENSP00000419868.1:n.530-12C>A
ENST00000489173.1:n.810C>A
XM_005264878.2:c.530-527C>A	XP_005264935.1:n.530-527C>A
XM_017005730.1:c.149-14C>A	XP_016861219.1:n.149-14C>A
XM_024453351.1:c.530-14C>A	XP_024309119.1:n.530-14C>A
XM_024453352.1:c.530-527C>A	XP_024309120.1:n.530-527C>A
XR_001740022.2:n.2432-14C>A
XR_001740023.2:n.2432-14C>A
XR_245095.2:n.2433-527C>A
XR_245095.4:n.2434-527C>A