Canonical Allele Identifier: CA1364789156

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292890T= , CM000665.2:g.52292890T=	GRCh38
NC_000003.11:g.52326906T= , CM000665.1:g.52326906T=	GRCh37
NC_000003.10:g.52301946T=	NCBI36
NG_023246.1:g.10071T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1336T= MANE Select	ENSP00000389175.2:p.Phe446=
ENST00000305690.12:c.*455T=	ENSP00000301965.9:n.*455T=
ENST00000436784.6:c.1336T=	ENSP00000389175.2:p.Phe446=
ENST00000461183.5:c.764-156T=	ENSP00000417264.1:n.764-156T=
ENST00000471180.5:c.635-156T=	ENSP00000417526.1:n.635-156T=
ENST00000473032.5:c.530-156T=	ENSP00000418951.1:n.530-156T=
ENST00000477382.1:c.*455T=	ENSP00000419008.1:n.*455T=
ENST00000486393.5:c.*699T=	ENSP00000419868.1:n.*699T=
ENST00000489173.1:n.1630T=
NM_001144951.1:c.*455T=	NP_001138423.1:n.*455T=
NM_145262.3:c.1336T=	NP_660305.2:p.Phe446=
NR_026699.1:n.1434T=
NR_026700.1:n.696-156T=
NR_026701.1:n.1432T=
NR_026702.1:n.626-156T=
XM_005264878.2:c.*455T=	XP_005264935.1:n.*455T=
XR_245095.2:n.2743-156T=
XM_017005730.1:c.955T=	XP_016861219.1:p.Phe319=
XM_024453351.1:c.1336T=	XP_024309119.1:p.Phe446=
XM_024453352.1:c.*455T=	XP_024309120.1:n.*455T=
XR_001740022.2:n.3238T=
XR_001740023.2:n.2918-156T=
XR_245095.4:n.2744-156T=
NM_145262.4:c.1336T= MANE Select	NP_660305.2:p.Phe446=
NR_026699.2:n.1426T=
NR_026700.2:n.688-156T=
NR_026701.2:n.1424T=
NR_026702.2:n.618-156T=
NM_001144951.2:c.*455T=	NP_001138423.1:n.*455T=