Canonical Allele Identifier: CA1364789043

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292651C= , CM000665.2:g.52292651C=	GRCh38
NC_000003.11:g.52326667C= , CM000665.1:g.52326667C=	GRCh37
NC_000003.10:g.52301707C=	NCBI36
NG_023246.1:g.9832C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1097C= MANE Select	ENSP00000389175.2:p.Ala366=
ENST00000305690.12:c.*216C=	ENSP00000301965.9:n.*216C=
ENST00000436784.6:c.1097C=	ENSP00000389175.2:p.Ala366=
ENST00000461183.5:c.763+82C=	ENSP00000417264.1:n.763+82C=
ENST00000471180.5:c.634+82C=	ENSP00000417526.1:n.634+82C=
ENST00000473032.5:c.530-395C=	ENSP00000418951.1:n.530-395C=
ENST00000477382.1:c.*216C=	ENSP00000419008.1:n.*216C=
ENST00000486393.5:c.*460C=	ENSP00000419868.1:n.*460C=
ENST00000489173.1:n.1391C=
NM_001144951.1:c.*216C=	NP_001138423.1:n.*216C=
NM_145262.3:c.1097C=	NP_660305.2:p.Ala366=
NR_026699.1:n.1195C=
NR_026700.1:n.695+82C=
NR_026701.1:n.1193C=
NR_026702.1:n.626-395C=
XM_005264878.2:c.*216C=	XP_005264935.1:n.*216C=
XR_245095.2:n.2742+82C=
XM_017005730.1:c.716C=	XP_016861219.1:p.Ala239=
XM_024453351.1:c.1097C=	XP_024309119.1:p.Ala366=
XM_024453352.1:c.*216C=	XP_024309120.1:n.*216C=
XR_001740022.2:n.2999C=
XR_001740023.2:n.2917+82C=
XR_245095.4:n.2743+82C=
NM_145262.4:c.1097C= MANE Select	NP_660305.2:p.Ala366=
NR_026699.2:n.1187C=
NR_026700.2:n.687+82C=
NR_026701.2:n.1185C=
NR_026702.2:n.618-395C=
NM_001144951.2:c.*216C=	NP_001138423.1:n.*216C=