Canonical Allele Identifier: CA1364789039

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292637A= , CM000665.2:g.52292637A=	GRCh38
NC_000003.11:g.52326653A= , CM000665.1:g.52326653A=	GRCh37
NC_000003.10:g.52301693A=	NCBI36
NG_023246.1:g.9818A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1083A= MANE Select	ENSP00000389175.2:p.Pro361=
ENST00000305690.12:c.*202A=	ENSP00000301965.9:n.*202A=
ENST00000436784.6:c.1083A=	ENSP00000389175.2:p.Pro361=
ENST00000461183.5:c.763+68A=	ENSP00000417264.1:n.763+68A=
ENST00000471180.5:c.634+68A=	ENSP00000417526.1:n.634+68A=
ENST00000473032.5:c.530-409A=	ENSP00000418951.1:n.530-409A=
ENST00000477382.1:c.*202A=	ENSP00000419008.1:n.*202A=
ENST00000486393.5:c.*446A=	ENSP00000419868.1:n.*446A=
ENST00000489173.1:n.1377A=
NM_001144951.1:c.*202A=	NP_001138423.1:n.*202A=
NM_145262.3:c.1083A=	NP_660305.2:p.Pro361=
NR_026699.1:n.1181A=
NR_026700.1:n.695+68A=
NR_026701.1:n.1179A=
NR_026702.1:n.626-409A=
XM_005264878.2:c.*202A=	XP_005264935.1:n.*202A=
XR_245095.2:n.2742+68A=
XM_017005730.1:c.702A=	XP_016861219.1:p.Pro234=
XM_024453351.1:c.1083A=	XP_024309119.1:p.Pro361=
XM_024453352.1:c.*202A=	XP_024309120.1:n.*202A=
XR_001740022.2:n.2985A=
XR_001740023.2:n.2917+68A=
XR_245095.4:n.2743+68A=
NM_145262.4:c.1083A= MANE Select	NP_660305.2:p.Pro361=
NR_026699.2:n.1173A=
NR_026700.2:n.687+68A=
NR_026701.2:n.1171A=
NR_026702.2:n.618-409A=
NM_001144951.2:c.*202A=	NP_001138423.1:n.*202A=