Canonical Allele Identifier: CA74735916

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52290379C>T , CM000665.2:g.52290379C>T	GRCh38
NC_000003.11:g.52324395C>T , CM000665.1:g.52324395C>T	GRCh37
NC_000003.10:g.52299435C>T	NCBI36
NG_023246.1:g.7560C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_145262.4:c.37C>T MANE Select	NP_660305.2:p.Arg13Ter
ENST00000436784.7:c.37C>T MANE Select	ENSP00000389175.2:p.Arg13Ter
NM_001144951.1:c.37C>T	NP_001138423.1:p.Arg13Ter
NM_001144951.2:c.37C>T	NP_001138423.1:p.Arg13Ter
NM_145262.3:c.37C>T	NP_660305.2:p.Arg13Ter
NR_026699.1:n.133C>T
NR_026699.2:n.125C>T
NR_026700.1:n.58-581C>T
NR_026700.2:n.50-581C>T
NR_026701.1:n.133C>T
NR_026701.2:n.125C>T
NR_026702.1:n.133C>T
NR_026702.2:n.125C>T
ENST00000305690.12:c.37C>T	ENSP00000301965.9:p.Arg13Ter
ENST00000436784.6:c.37C>T	ENSP00000389175.2:p.Arg13Ter
ENST00000461183.5:c.126-581C>T	ENSP00000417264.1:n.126-581C>T
ENST00000471180.5:c.-4-581C>T	ENSP00000417526.1:n.-4-581C>T
ENST00000473032.5:c.37C>T	ENSP00000418951.1:p.Arg13Ter
ENST00000473583.1:n.306C>T
ENST00000477382.1:c.37C>T	ENSP00000419008.1:p.Arg13Ter
ENST00000486393.5:c.37C>T	ENSP00000419868.1:p.Arg13Ter
XM_005264878.2:c.37C>T	XP_005264935.1:p.Arg13Ter
XM_017005730.1:c.-4-581C>T	XP_016861219.1:n.-4-581C>T
XM_024453351.1:c.37C>T	XP_024309119.1:p.Arg13Ter
XM_024453352.1:c.37C>T	XP_024309120.1:p.Arg13Ter
XR_001740022.2:n.1939C>T
XR_001740023.2:n.1939C>T
XR_245095.2:n.1940C>T
XR_245095.4:n.1941C>T