Canonical Allele Identifier: CA1364789034

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292624C= , CM000665.2:g.52292624C=	GRCh38
NC_000003.11:g.52326640C= , CM000665.1:g.52326640C=	GRCh37
NC_000003.10:g.52301680C=	NCBI36
NG_023246.1:g.9805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1070C= MANE Select	ENSP00000389175.2:p.Thr357=
ENST00000305690.12:c.*189C=	ENSP00000301965.9:n.*189C=
ENST00000436784.6:c.1070C=	ENSP00000389175.2:p.Thr357=
ENST00000461183.5:c.763+55C=	ENSP00000417264.1:n.763+55C=
ENST00000471180.5:c.634+55C=	ENSP00000417526.1:n.634+55C=
ENST00000473032.5:c.530-422C=	ENSP00000418951.1:n.530-422C=
ENST00000477382.1:c.*189C=	ENSP00000419008.1:n.*189C=
ENST00000486393.5:c.*433C=	ENSP00000419868.1:n.*433C=
ENST00000489173.1:n.1364C=
NM_001144951.1:c.*189C=	NP_001138423.1:n.*189C=
NM_145262.3:c.1070C=	NP_660305.2:p.Thr357=
NR_026699.1:n.1168C=
NR_026700.1:n.695+55C=
NR_026701.1:n.1166C=
NR_026702.1:n.626-422C=
XM_005264878.2:c.*189C=	XP_005264935.1:n.*189C=
XR_245095.2:n.2742+55C=
XM_017005730.1:c.689C=	XP_016861219.1:p.Thr230=
XM_024453351.1:c.1070C=	XP_024309119.1:p.Thr357=
XM_024453352.1:c.*189C=	XP_024309120.1:n.*189C=
XR_001740022.2:n.2972C=
XR_001740023.2:n.2917+55C=
XR_245095.4:n.2743+55C=
NM_145262.4:c.1070C= MANE Select	NP_660305.2:p.Thr357=
NR_026699.2:n.1160C=
NR_026700.2:n.687+55C=
NR_026701.2:n.1158C=
NR_026702.2:n.618-422C=
NM_001144951.2:c.*189C=	NP_001138423.1:n.*189C=