Canonical Allele Identifier: CA1364789020

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292603T= , CM000665.2:g.52292603T=	GRCh38
NC_000003.11:g.52326619T= , CM000665.1:g.52326619T=	GRCh37
NC_000003.10:g.52301659T=	NCBI36
NG_023246.1:g.9784T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1049T= MANE Select	ENSP00000389175.2:p.Leu350=
ENST00000305690.12:c.*168T=	ENSP00000301965.9:n.*168T=
ENST00000436784.6:c.1049T=	ENSP00000389175.2:p.Leu350=
ENST00000461183.5:c.763+34T=	ENSP00000417264.1:n.763+34T=
ENST00000471180.5:c.634+34T=	ENSP00000417526.1:n.634+34T=
ENST00000473032.5:c.530-443T=	ENSP00000418951.1:n.530-443T=
ENST00000477382.1:c.*168T=	ENSP00000419008.1:n.*168T=
ENST00000486393.5:c.*412T=	ENSP00000419868.1:n.*412T=
ENST00000489173.1:n.1343T=
NM_001144951.1:c.*168T=	NP_001138423.1:n.*168T=
NM_145262.3:c.1049T=	NP_660305.2:p.Leu350=
NR_026699.1:n.1147T=
NR_026700.1:n.695+34T=
NR_026701.1:n.1145T=
NR_026702.1:n.626-443T=
XM_005264878.2:c.*168T=	XP_005264935.1:n.*168T=
XR_245095.2:n.2742+34T=
XM_017005730.1:c.668T=	XP_016861219.1:p.Leu223=
XM_024453351.1:c.1049T=	XP_024309119.1:p.Leu350=
XM_024453352.1:c.*168T=	XP_024309120.1:n.*168T=
XR_001740022.2:n.2951T=
XR_001740023.2:n.2917+34T=
XR_245095.4:n.2743+34T=
NM_145262.4:c.1049T= MANE Select	NP_660305.2:p.Leu350=
NR_026699.2:n.1139T=
NR_026700.2:n.687+34T=
NR_026701.2:n.1137T=
NR_026702.2:n.618-443T=
NM_001144951.2:c.*168T=	NP_001138423.1:n.*168T=