Canonical Allele Identifier: CA1364789245

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293086A= , CM000665.2:g.52293086A=	GRCh38
NC_000003.11:g.52327102A= , CM000665.1:g.52327102A=	GRCh37
NC_000003.10:g.52302142A=	NCBI36
NG_023246.1:g.10267A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1532A= MANE Select	ENSP00000389175.2:p.Asn511=
ENST00000436784.6:c.1532A=	ENSP00000389175.2:p.Asn511=
ENST00000461183.5:c.804A=	ENSP00000417264.1:p.Gln268=
ENST00000471180.5:c.675A=	ENSP00000417526.1:p.Gln225=
ENST00000473032.5:c.570A=	ENSP00000418951.1:p.Gln190=
ENST00000486393.5:c.*895A=	ENSP00000419868.1:n.*895A=
ENST00000489173.1:n.1826A=
NM_145262.3:c.1532A=	NP_660305.2:p.Asn511=
NR_026699.1:n.1630A=
NR_026700.1:n.736A=
NR_026701.1:n.1628A=
NR_026702.1:n.666A=
XM_005264878.2:c.*651A=	XP_005264935.1:n.*651A=
XR_245095.2:n.2783A=
XM_017005730.1:c.1151A=	XP_016861219.1:p.Asn384=
XM_024453351.1:c.1532A=	XP_024309119.1:p.Asn511=
XM_024453352.1:c.*651A=	XP_024309120.1:n.*651A=
XR_001740022.2:n.3434A=
XR_001740023.2:n.2958A=
XR_245095.4:n.2784A=
NM_145262.4:c.1532A= MANE Select	NP_660305.2:p.Asn511=
NR_026699.2:n.1622A=
NR_026700.2:n.728A=
NR_026701.2:n.1620A=
NR_026702.2:n.658A=
NM_001144951.2:c.*651A=	NP_001138423.1:n.*651A=