Canonical Allele Identifier: CA1364789013

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292595C= , CM000665.2:g.52292595C=	GRCh38
NC_000003.11:g.52326611C= , CM000665.1:g.52326611C=	GRCh37
NC_000003.10:g.52301651C=	NCBI36
NG_023246.1:g.9776C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1041C= MANE Select	ENSP00000389175.2:p.Phe347=
ENST00000305690.12:c.*160C=	ENSP00000301965.9:n.*160C=
ENST00000436784.6:c.1041C=	ENSP00000389175.2:p.Phe347=
ENST00000461183.5:c.763+26C=	ENSP00000417264.1:n.763+26C=
ENST00000471180.5:c.634+26C=	ENSP00000417526.1:n.634+26C=
ENST00000473032.5:c.530-451C=	ENSP00000418951.1:n.530-451C=
ENST00000477382.1:c.*160C=	ENSP00000419008.1:n.*160C=
ENST00000486393.5:c.*404C=	ENSP00000419868.1:n.*404C=
ENST00000489173.1:n.1335C=
NM_001144951.1:c.*160C=	NP_001138423.1:n.*160C=
NM_145262.3:c.1041C=	NP_660305.2:p.Phe347=
NR_026699.1:n.1139C=
NR_026700.1:n.695+26C=
NR_026701.1:n.1137C=
NR_026702.1:n.626-451C=
XM_005264878.2:c.*160C=	XP_005264935.1:n.*160C=
XR_245095.2:n.2742+26C=
XM_017005730.1:c.660C=	XP_016861219.1:p.Phe220=
XM_024453351.1:c.1041C=	XP_024309119.1:p.Phe347=
XM_024453352.1:c.*160C=	XP_024309120.1:n.*160C=
XR_001740022.2:n.2943C=
XR_001740023.2:n.2917+26C=
XR_245095.4:n.2743+26C=
NM_145262.4:c.1041C= MANE Select	NP_660305.2:p.Phe347=
NR_026699.2:n.1131C=
NR_026700.2:n.687+26C=
NR_026701.2:n.1129C=
NR_026702.2:n.618-451C=
NM_001144951.2:c.*160C=	NP_001138423.1:n.*160C=