Canonical Allele Identifier: CA1364789016

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292599G= , CM000665.2:g.52292599G=	GRCh38
NC_000003.11:g.52326615G= , CM000665.1:g.52326615G=	GRCh37
NC_000003.10:g.52301655G=	NCBI36
NG_023246.1:g.9780G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1045G= MANE Select	ENSP00000389175.2:p.Gly349=
ENST00000305690.12:c.*164G=	ENSP00000301965.9:n.*164G=
ENST00000436784.6:c.1045G=	ENSP00000389175.2:p.Gly349=
ENST00000461183.5:c.763+30G=	ENSP00000417264.1:n.763+30G=
ENST00000471180.5:c.634+30G=	ENSP00000417526.1:n.634+30G=
ENST00000473032.5:c.530-447G=	ENSP00000418951.1:n.530-447G=
ENST00000477382.1:c.*164G=	ENSP00000419008.1:n.*164G=
ENST00000486393.5:c.*408G=	ENSP00000419868.1:n.*408G=
ENST00000489173.1:n.1339G=
NM_001144951.1:c.*164G=	NP_001138423.1:n.*164G=
NM_145262.3:c.1045G=	NP_660305.2:p.Gly349=
NR_026699.1:n.1143G=
NR_026700.1:n.695+30G=
NR_026701.1:n.1141G=
NR_026702.1:n.626-447G=
XM_005264878.2:c.*164G=	XP_005264935.1:n.*164G=
XR_245095.2:n.2742+30G=
XM_017005730.1:c.664G=	XP_016861219.1:p.Gly222=
XM_024453351.1:c.1045G=	XP_024309119.1:p.Gly349=
XM_024453352.1:c.*164G=	XP_024309120.1:n.*164G=
XR_001740022.2:n.2947G=
XR_001740023.2:n.2917+30G=
XR_245095.4:n.2743+30G=
NM_145262.4:c.1045G= MANE Select	NP_660305.2:p.Gly349=
NR_026699.2:n.1135G=
NR_026700.2:n.687+30G=
NR_026701.2:n.1133G=
NR_026702.2:n.618-447G=
NM_001144951.2:c.*164G=	NP_001138423.1:n.*164G=