Canonical Allele Identifier: CA1364789260

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293116G= , CM000665.2:g.52293116G=	GRCh38
NC_000003.11:g.52327132G= , CM000665.1:g.52327132G=	GRCh37
NC_000003.10:g.52302172G=	NCBI36
NG_023246.1:g.10297G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1562G= MANE Select	ENSP00000389175.2:p.Arg521=
ENST00000436784.6:c.1562G=	ENSP00000389175.2:p.Arg521=
ENST00000461183.5:c.834G=	ENSP00000417264.1:p.Ala278=
ENST00000471180.5:c.705G=	ENSP00000417526.1:p.Ala235=
ENST00000473032.5:c.600G=	ENSP00000418951.1:p.Ala200=
ENST00000486393.5:c.*925G=	ENSP00000419868.1:n.*925G=
ENST00000489173.1:n.1856G=
NM_145262.3:c.1562G=	NP_660305.2:p.Arg521=
NR_026699.1:n.1660G=
NR_026700.1:n.766G=
NR_026701.1:n.1658G=
NR_026702.1:n.696G=
XM_005264878.2:c.*681G=	XP_005264935.1:n.*681G=
XR_245095.2:n.2813G=
XM_017005730.1:c.1181G=	XP_016861219.1:p.Arg394=
XM_024453351.1:c.1562G=	XP_024309119.1:p.Arg521=
XM_024453352.1:c.*681G=	XP_024309120.1:n.*681G=
XR_001740022.2:n.3464G=
XR_001740023.2:n.2988G=
XR_245095.4:n.2814G=
NM_145262.4:c.1562G= MANE Select	NP_660305.2:p.Arg521=
NR_026699.2:n.1652G=
NR_026700.2:n.758G=
NR_026701.2:n.1650G=
NR_026702.2:n.688G=
NM_001144951.2:c.*681G=	NP_001138423.1:n.*681G=