Canonical Allele Identifier: CA1364789266

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293128G= , CM000665.2:g.52293128G=	GRCh38
NC_000003.11:g.52327144G= , CM000665.1:g.52327144G=	GRCh37
NC_000003.10:g.52302184G=	NCBI36
NG_023246.1:g.10309G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*2G= MANE Select	ENSP00000389175.2:n.*2G=
ENST00000436784.6:c.*2G=	ENSP00000389175.2:n.*2G=
ENST00000461183.5:c.846G=	ENSP00000417264.1:p.Met282=
ENST00000471180.5:c.717G=	ENSP00000417526.1:p.Met239=
ENST00000473032.5:c.612G=	ENSP00000418951.1:p.Met204=
ENST00000486393.5:c.*937G=	ENSP00000419868.1:n.*937G=
ENST00000489173.1:n.1868G=
NM_145262.3:c.*2G=	NP_660305.2:n.*2G=
NR_026699.1:n.1672G=
NR_026700.1:n.778G=
NR_026701.1:n.1670G=
NR_026702.1:n.708G=
XM_005264878.2:c.*693G=	XP_005264935.1:n.*693G=
XR_245095.2:n.2825G=
XM_017005730.1:c.*2G=	XP_016861219.1:n.*2G=
XM_024453351.1:c.*2G=	XP_024309119.1:n.*2G=
XM_024453352.1:c.*693G=	XP_024309120.1:n.*693G=
XR_001740022.2:n.3476G=
XR_001740023.2:n.3000G=
XR_245095.4:n.2826G=
NM_145262.4:c.*2G= MANE Select	NP_660305.2:n.*2G=
NR_026699.2:n.1664G=
NR_026700.2:n.770G=
NR_026701.2:n.1662G=
NR_026702.2:n.700G=
NM_001144951.2:c.*693G=	NP_001138423.1:n.*693G=