Canonical Allele Identifier: CA1364789246

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293088G= , CM000665.2:g.52293088G=	GRCh38
NC_000003.11:g.52327104G= , CM000665.1:g.52327104G=	GRCh37
NC_000003.10:g.52302144G=	NCBI36
NG_023246.1:g.10269G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1534G= MANE Select	ENSP00000389175.2:p.Val512=
ENST00000436784.6:c.1534G=	ENSP00000389175.2:p.Val512=
ENST00000461183.5:c.806G=	ENSP00000417264.1:p.Cys269=
ENST00000471180.5:c.677G=	ENSP00000417526.1:p.Cys226=
ENST00000473032.5:c.572G=	ENSP00000418951.1:p.Cys191=
ENST00000486393.5:c.*897G=	ENSP00000419868.1:n.*897G=
ENST00000489173.1:n.1828G=
NM_145262.3:c.1534G=	NP_660305.2:p.Val512=
NR_026699.1:n.1632G=
NR_026700.1:n.738G=
NR_026701.1:n.1630G=
NR_026702.1:n.668G=
XM_005264878.2:c.*653G=	XP_005264935.1:n.*653G=
XR_245095.2:n.2785G=
XM_017005730.1:c.1153G=	XP_016861219.1:p.Val385=
XM_024453351.1:c.1534G=	XP_024309119.1:p.Val512=
XM_024453352.1:c.*653G=	XP_024309120.1:n.*653G=
XR_001740022.2:n.3436G=
XR_001740023.2:n.2960G=
XR_245095.4:n.2786G=
NM_145262.4:c.1534G= MANE Select	NP_660305.2:p.Val512=
NR_026699.2:n.1624G=
NR_026700.2:n.730G=
NR_026701.2:n.1622G=
NR_026702.2:n.660G=
NM_001144951.2:c.*653G=	NP_001138423.1:n.*653G=