Canonical Allele Identifier: CA74736634

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292451C>T , CM000665.2:g.52292451C>T	GRCh38
NC_000003.11:g.52326467C>T , CM000665.1:g.52326467C>T	GRCh37
NC_000003.10:g.52301507C>T	NCBI36
NG_023246.1:g.9632C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.897C>T MANE Select	ENSP00000389175.2:p.His299=
ENST00000305690.12:c.*16C>T	ENSP00000301965.9:n.*16C>T
ENST00000436784.6:c.897C>T	ENSP00000389175.2:p.His299=
ENST00000461183.5:c.645C>T	ENSP00000417264.1:p.His215=
ENST00000471180.5:c.516C>T	ENSP00000417526.1:p.His172=
ENST00000473032.5:c.530-595C>T	ENSP00000418951.1:n.530-595C>T
ENST00000473583.1:n.990C>T
ENST00000477382.1:c.*16C>T	ENSP00000419008.1:n.*16C>T
ENST00000486393.5:c.*260C>T	ENSP00000419868.1:n.*260C>T
ENST00000489173.1:n.1191C>T
NM_001144951.1:c.*16C>T	NP_001138423.1:n.*16C>T
NM_145262.3:c.897C>T	NP_660305.2:p.His299=
NR_026699.1:n.995C>T
NR_026700.1:n.577C>T
NR_026701.1:n.993C>T
NR_026702.1:n.626-595C>T
XM_005264878.2:c.*16C>T	XP_005264935.1:n.*16C>T
XR_245095.2:n.2624C>T
XM_017005730.1:c.516C>T	XP_016861219.1:p.His172=
XM_024453351.1:c.897C>T	XP_024309119.1:p.His299=
XM_024453352.1:c.*16C>T	XP_024309120.1:n.*16C>T
XR_001740022.2:n.2799C>T
XR_001740023.2:n.2799C>T
XR_245095.4:n.2625C>T
NM_145262.4:c.897C>T MANE Select	NP_660305.2:p.His299=
NR_026699.2:n.987C>T
NR_026700.2:n.569C>T
NR_026701.2:n.985C>T
NR_026702.2:n.618-595C>T
NM_001144951.2:c.*16C>T	NP_001138423.1:n.*16C>T