Canonical Allele Identifier: CA1364789018

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292601G= , CM000665.2:g.52292601G=	GRCh38
NC_000003.11:g.52326617G= , CM000665.1:g.52326617G=	GRCh37
NC_000003.10:g.52301657G=	NCBI36
NG_023246.1:g.9782G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1047G= MANE Select	ENSP00000389175.2:p.Gly349=
ENST00000305690.12:c.*166G=	ENSP00000301965.9:n.*166G=
ENST00000436784.6:c.1047G=	ENSP00000389175.2:p.Gly349=
ENST00000461183.5:c.763+32G=	ENSP00000417264.1:n.763+32G=
ENST00000471180.5:c.634+32G=	ENSP00000417526.1:n.634+32G=
ENST00000473032.5:c.530-445G=	ENSP00000418951.1:n.530-445G=
ENST00000477382.1:c.*166G=	ENSP00000419008.1:n.*166G=
ENST00000486393.5:c.*410G=	ENSP00000419868.1:n.*410G=
ENST00000489173.1:n.1341G=
NM_001144951.1:c.*166G=	NP_001138423.1:n.*166G=
NM_145262.3:c.1047G=	NP_660305.2:p.Gly349=
NR_026699.1:n.1145G=
NR_026700.1:n.695+32G=
NR_026701.1:n.1143G=
NR_026702.1:n.626-445G=
XM_005264878.2:c.*166G=	XP_005264935.1:n.*166G=
XR_245095.2:n.2742+32G=
XM_017005730.1:c.666G=	XP_016861219.1:p.Gly222=
XM_024453351.1:c.1047G=	XP_024309119.1:p.Gly349=
XM_024453352.1:c.*166G=	XP_024309120.1:n.*166G=
XR_001740022.2:n.2949G=
XR_001740023.2:n.2917+32G=
XR_245095.4:n.2743+32G=
NM_145262.4:c.1047G= MANE Select	NP_660305.2:p.Gly349=
NR_026699.2:n.1137G=
NR_026700.2:n.687+32G=
NR_026701.2:n.1135G=
NR_026702.2:n.618-445G=
NM_001144951.2:c.*166G=	NP_001138423.1:n.*166G=