Canonical Allele Identifier: CA1364789267

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293129G= , CM000665.2:g.52293129G=	GRCh38
NC_000003.11:g.52327145G= , CM000665.1:g.52327145G=	GRCh37
NC_000003.10:g.52302185G=	NCBI36
NG_023246.1:g.10310G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*3G= MANE Select	ENSP00000389175.2:n.*3G=
ENST00000436784.6:c.*3G=	ENSP00000389175.2:n.*3G=
ENST00000461183.5:c.847G=	ENSP00000417264.1:p.Ala283=
ENST00000471180.5:c.718G=	ENSP00000417526.1:p.Ala240=
ENST00000473032.5:c.613G=	ENSP00000418951.1:p.Ala205=
ENST00000486393.5:c.*938G=	ENSP00000419868.1:n.*938G=
ENST00000489173.1:n.1869G=
NM_145262.3:c.*3G=	NP_660305.2:n.*3G=
NR_026699.1:n.1673G=
NR_026700.1:n.779G=
NR_026701.1:n.1671G=
NR_026702.1:n.709G=
XM_005264878.2:c.*694G=	XP_005264935.1:n.*694G=
XR_245095.2:n.2826G=
XM_017005730.1:c.*3G=	XP_016861219.1:n.*3G=
XM_024453351.1:c.*3G=	XP_024309119.1:n.*3G=
XM_024453352.1:c.*694G=	XP_024309120.1:n.*694G=
XR_001740022.2:n.3477G=
XR_001740023.2:n.3001G=
XR_245095.4:n.2827G=
NM_145262.4:c.*3G= MANE Select	NP_660305.2:n.*3G=
NR_026699.2:n.1665G=
NR_026700.2:n.771G=
NR_026701.2:n.1663G=
NR_026702.2:n.701G=
NM_001144951.2:c.*694G=	NP_001138423.1:n.*694G=