Canonical Allele Identifier: CA1364789050

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292674C= , CM000665.2:g.52292674C=	GRCh38
NC_000003.11:g.52326690C= , CM000665.1:g.52326690C=	GRCh37
NC_000003.10:g.52301730C=	NCBI36
NG_023246.1:g.9855C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1120C= MANE Select	ENSP00000389175.2:p.Leu374=
ENST00000305690.12:c.*239C=	ENSP00000301965.9:n.*239C=
ENST00000436784.6:c.1120C=	ENSP00000389175.2:p.Leu374=
ENST00000461183.5:c.763+105C=	ENSP00000417264.1:n.763+105C=
ENST00000471180.5:c.634+105C=	ENSP00000417526.1:n.634+105C=
ENST00000473032.5:c.530-372C=	ENSP00000418951.1:n.530-372C=
ENST00000477382.1:c.*239C=	ENSP00000419008.1:n.*239C=
ENST00000486393.5:c.*483C=	ENSP00000419868.1:n.*483C=
ENST00000489173.1:n.1414C=
NM_001144951.1:c.*239C=	NP_001138423.1:n.*239C=
NM_145262.3:c.1120C=	NP_660305.2:p.Leu374=
NR_026699.1:n.1218C=
NR_026700.1:n.695+105C=
NR_026701.1:n.1216C=
NR_026702.1:n.626-372C=
XM_005264878.2:c.*239C=	XP_005264935.1:n.*239C=
XR_245095.2:n.2742+105C=
XM_017005730.1:c.739C=	XP_016861219.1:p.Leu247=
XM_024453351.1:c.1120C=	XP_024309119.1:p.Leu374=
XM_024453352.1:c.*239C=	XP_024309120.1:n.*239C=
XR_001740022.2:n.3022C=
XR_001740023.2:n.2917+105C=
XR_245095.4:n.2743+105C=
NM_145262.4:c.1120C= MANE Select	NP_660305.2:p.Leu374=
NR_026699.2:n.1210C=
NR_026700.2:n.687+105C=
NR_026701.2:n.1208C=
NR_026702.2:n.618-372C=
NM_001144951.2:c.*239C=	NP_001138423.1:n.*239C=