Canonical Allele Identifier: CA1364789068

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292716C= , CM000665.2:g.52292716C=	GRCh38
NC_000003.11:g.52326732C= , CM000665.1:g.52326732C=	GRCh37
NC_000003.10:g.52301772C=	NCBI36
NG_023246.1:g.9897C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1162C= MANE Select	ENSP00000389175.2:p.Leu388=
ENST00000305690.12:c.*281C=	ENSP00000301965.9:n.*281C=
ENST00000436784.6:c.1162C=	ENSP00000389175.2:p.Leu388=
ENST00000461183.5:c.763+147C=	ENSP00000417264.1:n.763+147C=
ENST00000471180.5:c.634+147C=	ENSP00000417526.1:n.634+147C=
ENST00000473032.5:c.530-330C=	ENSP00000418951.1:n.530-330C=
ENST00000477382.1:c.*281C=	ENSP00000419008.1:n.*281C=
ENST00000486393.5:c.*525C=	ENSP00000419868.1:n.*525C=
ENST00000489173.1:n.1456C=
NM_001144951.1:c.*281C=	NP_001138423.1:n.*281C=
NM_145262.3:c.1162C=	NP_660305.2:p.Leu388=
NR_026699.1:n.1260C=
NR_026700.1:n.695+147C=
NR_026701.1:n.1258C=
NR_026702.1:n.626-330C=
XM_005264878.2:c.*281C=	XP_005264935.1:n.*281C=
XR_245095.2:n.2742+147C=
XM_017005730.1:c.781C=	XP_016861219.1:p.Leu261=
XM_024453351.1:c.1162C=	XP_024309119.1:p.Leu388=
XM_024453352.1:c.*281C=	XP_024309120.1:n.*281C=
XR_001740022.2:n.3064C=
XR_001740023.2:n.2917+147C=
XR_245095.4:n.2743+147C=
NM_145262.4:c.1162C= MANE Select	NP_660305.2:p.Leu388=
NR_026699.2:n.1252C=
NR_026700.2:n.687+147C=
NR_026701.2:n.1250C=
NR_026702.2:n.618-330C=
NM_001144951.2:c.*281C=	NP_001138423.1:n.*281C=