Canonical Allele Identifier: CA1364789313

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293214A= , CM000665.2:g.52293214A=	GRCh38
NC_000003.11:g.52327230A= , CM000665.1:g.52327230A=	GRCh37
NC_000003.10:g.52302270A=	NCBI36
NG_023246.1:g.10395A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*88A= MANE Select	ENSP00000389175.2:n.*88A=
ENST00000436784.6:c.*88A=	ENSP00000389175.2:n.*88A=
ENST00000471180.5:c.*58+22A=	ENSP00000417526.1:n.*58+22A=
ENST00000473032.5:c.*58+22A=	ENSP00000418951.1:n.*58+22A=
ENST00000486393.5:c.*1023A=	ENSP00000419868.1:n.*1023A=
ENST00000489173.1:n.1914+40A=
NM_145262.3:c.*88A=	NP_660305.2:n.*88A=
NR_026699.1:n.1758A=
NR_026700.1:n.842+22A=
NR_026701.1:n.1734+22A=
NR_026702.1:n.772+22A=
XM_005264878.2:c.*779A=	XP_005264935.1:n.*779A=
XR_245095.2:n.2889+22A=
XM_017005730.1:c.*88A=	XP_016861219.1:n.*88A=
XM_024453351.1:c.*88A=	XP_024309119.1:n.*88A=
XM_024453352.1:c.*779A=	XP_024309120.1:n.*779A=
XR_001740022.2:n.3540+22A=
XR_001740023.2:n.3064+22A=
XR_245095.4:n.2890+22A=
NM_145262.4:c.*88A= MANE Select	NP_660305.2:n.*88A=
NR_026699.2:n.1750A=
NR_026700.2:n.834+22A=
NR_026701.2:n.1726+22A=
NR_026702.2:n.764+22A=
NM_001144951.2:c.*779A=	NP_001138423.1:n.*779A=