Canonical Allele Identifier: CA1364789255

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293108G= , CM000665.2:g.52293108G=	GRCh38
NC_000003.11:g.52327124G= , CM000665.1:g.52327124G=	GRCh37
NC_000003.10:g.52302164G=	NCBI36
NG_023246.1:g.10289G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1554G= MANE Select	ENSP00000389175.2:p.Leu518=
ENST00000436784.6:c.1554G=	ENSP00000389175.2:p.Leu518=
ENST00000461183.5:c.826G=	ENSP00000417264.1:p.Val276=
ENST00000471180.5:c.697G=	ENSP00000417526.1:p.Val233=
ENST00000473032.5:c.592G=	ENSP00000418951.1:p.Val198=
ENST00000486393.5:c.*917G=	ENSP00000419868.1:n.*917G=
ENST00000489173.1:n.1848G=
NM_145262.3:c.1554G=	NP_660305.2:p.Leu518=
NR_026699.1:n.1652G=
NR_026700.1:n.758G=
NR_026701.1:n.1650G=
NR_026702.1:n.688G=
XM_005264878.2:c.*673G=	XP_005264935.1:n.*673G=
XR_245095.2:n.2805G=
XM_017005730.1:c.1173G=	XP_016861219.1:p.Leu391=
XM_024453351.1:c.1554G=	XP_024309119.1:p.Leu518=
XM_024453352.1:c.*673G=	XP_024309120.1:n.*673G=
XR_001740022.2:n.3456G=
XR_001740023.2:n.2980G=
XR_245095.4:n.2806G=
NM_145262.4:c.1554G= MANE Select	NP_660305.2:p.Leu518=
NR_026699.2:n.1644G=
NR_026700.2:n.750G=
NR_026701.2:n.1642G=
NR_026702.2:n.680G=
NM_001144951.2:c.*673G=	NP_001138423.1:n.*673G=