Canonical Allele Identifier: CA353074861

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326628A>T (hg19) ; chr3:g.52292612A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292612A>T , CM000665.2:g.52292612A>T	GRCh38
NC_000003.11:g.52326628A>T , CM000665.1:g.52326628A>T	GRCh37
NC_000003.10:g.52301668A>T	NCBI36
NG_023246.1:g.9793A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1058A>T MANE Select	ENSP00000389175.2:p.His353Leu
ENST00000305690.12:c.*177A>T	ENSP00000301965.9:n.*177A>T
ENST00000436784.6:c.1058A>T	ENSP00000389175.2:p.His353Leu
ENST00000461183.5:c.763+43A>T	ENSP00000417264.1:n.763+43A>T
ENST00000471180.5:c.634+43A>T	ENSP00000417526.1:n.634+43A>T
ENST00000473032.5:c.530-434A>T	ENSP00000418951.1:n.530-434A>T
ENST00000477382.1:c.*177A>T	ENSP00000419008.1:n.*177A>T
ENST00000486393.5:c.*421A>T	ENSP00000419868.1:n.*421A>T
ENST00000489173.1:n.1352A>T
NM_001144951.1:c.*177A>T	NP_001138423.1:n.*177A>T
NM_145262.3:c.1058A>T	NP_660305.2:p.His353Leu
NR_026699.1:n.1156A>T
NR_026700.1:n.695+43A>T
NR_026701.1:n.1154A>T
NR_026702.1:n.626-434A>T
XM_005264878.2:c.*177A>T	XP_005264935.1:n.*177A>T
XR_245095.2:n.2742+43A>T
XM_017005730.1:c.677A>T	XP_016861219.1:p.His226Leu
XM_024453351.1:c.1058A>T	XP_024309119.1:p.His353Leu
XM_024453352.1:c.*177A>T	XP_024309120.1:n.*177A>T
XR_001740022.2:n.2960A>T
XR_001740023.2:n.2917+43A>T
XR_245095.4:n.2743+43A>T
NM_145262.4:c.1058A>T MANE Select	NP_660305.2:p.His353Leu
NR_026699.2:n.1148A>T
NR_026700.2:n.687+43A>T
NR_026701.2:n.1146A>T
NR_026702.2:n.618-434A>T
NM_001144951.2:c.*177A>T	NP_001138423.1:n.*177A>T