Canonical Allele Identifier: CA1364789248

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293092T= , CM000665.2:g.52293092T=	GRCh38
NC_000003.11:g.52327108T= , CM000665.1:g.52327108T=	GRCh37
NC_000003.10:g.52302148T=	NCBI36
NG_023246.1:g.10273T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1538T= MANE Select	ENSP00000389175.2:p.Met513=
ENST00000436784.6:c.1538T=	ENSP00000389175.2:p.Met513=
ENST00000461183.5:c.810T=	ENSP00000417264.1:p.His270=
ENST00000471180.5:c.681T=	ENSP00000417526.1:p.His227=
ENST00000473032.5:c.576T=	ENSP00000418951.1:p.His192=
ENST00000486393.5:c.*901T=	ENSP00000419868.1:n.*901T=
ENST00000489173.1:n.1832T=
NM_145262.3:c.1538T=	NP_660305.2:p.Met513=
NR_026699.1:n.1636T=
NR_026700.1:n.742T=
NR_026701.1:n.1634T=
NR_026702.1:n.672T=
XM_005264878.2:c.*657T=	XP_005264935.1:n.*657T=
XR_245095.2:n.2789T=
XM_017005730.1:c.1157T=	XP_016861219.1:p.Met386=
XM_024453351.1:c.1538T=	XP_024309119.1:p.Met513=
XM_024453352.1:c.*657T=	XP_024309120.1:n.*657T=
XR_001740022.2:n.3440T=
XR_001740023.2:n.2964T=
XR_245095.4:n.2790T=
NM_145262.4:c.1538T= MANE Select	NP_660305.2:p.Met513=
NR_026699.2:n.1628T=
NR_026700.2:n.734T=
NR_026701.2:n.1626T=
NR_026702.2:n.664T=
NM_001144951.2:c.*657T=	NP_001138423.1:n.*657T=