Canonical Allele Identifier: CA1364789258

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293114G= , CM000665.2:g.52293114G=	GRCh38
NC_000003.11:g.52327130G= , CM000665.1:g.52327130G=	GRCh37
NC_000003.10:g.52302170G=	NCBI36
NG_023246.1:g.10295G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1560G= MANE Select	ENSP00000389175.2:p.Leu520=
ENST00000436784.6:c.1560G=	ENSP00000389175.2:p.Leu520=
ENST00000461183.5:c.832G=	ENSP00000417264.1:p.Ala278=
ENST00000471180.5:c.703G=	ENSP00000417526.1:p.Ala235=
ENST00000473032.5:c.598G=	ENSP00000418951.1:p.Ala200=
ENST00000486393.5:c.*923G=	ENSP00000419868.1:n.*923G=
ENST00000489173.1:n.1854G=
NM_145262.3:c.1560G=	NP_660305.2:p.Leu520=
NR_026699.1:n.1658G=
NR_026700.1:n.764G=
NR_026701.1:n.1656G=
NR_026702.1:n.694G=
XM_005264878.2:c.*679G=	XP_005264935.1:n.*679G=
XR_245095.2:n.2811G=
XM_017005730.1:c.1179G=	XP_016861219.1:p.Leu393=
XM_024453351.1:c.1560G=	XP_024309119.1:p.Leu520=
XM_024453352.1:c.*679G=	XP_024309120.1:n.*679G=
XR_001740022.2:n.3462G=
XR_001740023.2:n.2986G=
XR_245095.4:n.2812G=
NM_145262.4:c.1560G= MANE Select	NP_660305.2:p.Leu520=
NR_026699.2:n.1650G=
NR_026700.2:n.756G=
NR_026701.2:n.1648G=
NR_026702.2:n.686G=
NM_001144951.2:c.*679G=	NP_001138423.1:n.*679G=