Canonical Allele Identifier: CA1364789061

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292708A= , CM000665.2:g.52292708A=	GRCh38
NC_000003.11:g.52326724A= , CM000665.1:g.52326724A=	GRCh37
NC_000003.10:g.52301764A=	NCBI36
NG_023246.1:g.9889A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1154A= MANE Select	ENSP00000389175.2:p.Asp385=
ENST00000305690.12:c.*273A=	ENSP00000301965.9:n.*273A=
ENST00000436784.6:c.1154A=	ENSP00000389175.2:p.Asp385=
ENST00000461183.5:c.763+139A=	ENSP00000417264.1:n.763+139A=
ENST00000471180.5:c.634+139A=	ENSP00000417526.1:n.634+139A=
ENST00000473032.5:c.530-338A=	ENSP00000418951.1:n.530-338A=
ENST00000477382.1:c.*273A=	ENSP00000419008.1:n.*273A=
ENST00000486393.5:c.*517A=	ENSP00000419868.1:n.*517A=
ENST00000489173.1:n.1448A=
NM_001144951.1:c.*273A=	NP_001138423.1:n.*273A=
NM_145262.3:c.1154A=	NP_660305.2:p.Asp385=
NR_026699.1:n.1252A=
NR_026700.1:n.695+139A=
NR_026701.1:n.1250A=
NR_026702.1:n.626-338A=
XM_005264878.2:c.*273A=	XP_005264935.1:n.*273A=
XR_245095.2:n.2742+139A=
XM_017005730.1:c.773A=	XP_016861219.1:p.Asp258=
XM_024453351.1:c.1154A=	XP_024309119.1:p.Asp385=
XM_024453352.1:c.*273A=	XP_024309120.1:n.*273A=
XR_001740022.2:n.3056A=
XR_001740023.2:n.2917+139A=
XR_245095.4:n.2743+139A=
NM_145262.4:c.1154A= MANE Select	NP_660305.2:p.Asp385=
NR_026699.2:n.1244A=
NR_026700.2:n.687+139A=
NR_026701.2:n.1242A=
NR_026702.2:n.618-338A=
NM_001144951.2:c.*273A=	NP_001138423.1:n.*273A=