Canonical Allele Identifier: CA433882788

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326851C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292835C>A , CM000665.2:g.52292835C>A	GRCh38
NC_000003.11:g.52326851C>A , CM000665.1:g.52326851C>A	GRCh37
NC_000003.10:g.52301891C>A	NCBI36
NG_023246.1:g.10016C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1281C>A MANE Select	ENSP00000389175.2:p.Ala427=
ENST00000305690.12:c.*400C>A	ENSP00000301965.9:n.*400C>A
ENST00000436784.6:c.1281C>A	ENSP00000389175.2:p.Ala427=
ENST00000461183.5:c.764-211C>A	ENSP00000417264.1:n.764-211C>A
ENST00000471180.5:c.635-211C>A	ENSP00000417526.1:n.635-211C>A
ENST00000473032.5:c.530-211C>A	ENSP00000418951.1:n.530-211C>A
ENST00000477382.1:c.*400C>A	ENSP00000419008.1:n.*400C>A
ENST00000486393.5:c.*644C>A	ENSP00000419868.1:n.*644C>A
ENST00000489173.1:n.1575C>A
NM_001144951.1:c.*400C>A	NP_001138423.1:n.*400C>A
NM_145262.3:c.1281C>A	NP_660305.2:p.Ala427=
NR_026699.1:n.1379C>A
NR_026700.1:n.696-211C>A
NR_026701.1:n.1377C>A
NR_026702.1:n.626-211C>A
XM_005264878.2:c.*400C>A	XP_005264935.1:n.*400C>A
XR_245095.2:n.2743-211C>A
XM_017005730.1:c.900C>A	XP_016861219.1:p.Ala300=
XM_024453351.1:c.1281C>A	XP_024309119.1:p.Ala427=
XM_024453352.1:c.*400C>A	XP_024309120.1:n.*400C>A
XR_001740022.2:n.3183C>A
XR_001740023.2:n.2918-211C>A
XR_245095.4:n.2744-211C>A
NM_145262.4:c.1281C>A MANE Select	NP_660305.2:p.Ala427=
NR_026699.2:n.1371C>A
NR_026700.2:n.688-211C>A
NR_026701.2:n.1369C>A
NR_026702.2:n.618-211C>A
NM_001144951.2:c.*400C>A	NP_001138423.1:n.*400C>A