Canonical Allele Identifier: CA353076997

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327149A>T (hg19) ; chr3:g.52293133A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293133A>T , CM000665.2:g.52293133A>T	GRCh38
NC_000003.11:g.52327149A>T , CM000665.1:g.52327149A>T	GRCh37
NC_000003.10:g.52302189A>T	NCBI36
NG_023246.1:g.10314A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.*7A>T MANE Select	ENSP00000389175.2:n.*7A>T
ENST00000436784.6:c.*7A>T	ENSP00000389175.2:n.*7A>T
ENST00000461183.5:c.851A>T	ENSP00000417264.1:p.Ter284Leu
ENST00000471180.5:c.722A>T	ENSP00000417526.1:p.Ter241Leu
ENST00000473032.5:c.617A>T	ENSP00000418951.1:p.Ter206Leu
ENST00000486393.5:c.*942A>T	ENSP00000419868.1:n.*942A>T
ENST00000489173.1:n.1873A>T
NM_145262.3:c.*7A>T	NP_660305.2:n.*7A>T
NR_026699.1:n.1677A>T
NR_026700.1:n.783A>T
NR_026701.1:n.1675A>T
NR_026702.1:n.713A>T
XM_005264878.2:c.*698A>T	XP_005264935.1:n.*698A>T
XR_245095.2:n.2830A>T
XM_017005730.1:c.*7A>T	XP_016861219.1:n.*7A>T
XM_024453351.1:c.*7A>T	XP_024309119.1:n.*7A>T
XM_024453352.1:c.*698A>T	XP_024309120.1:n.*698A>T
XR_001740022.2:n.3481A>T
XR_001740023.2:n.3005A>T
XR_245095.4:n.2831A>T
NM_145262.4:c.*7A>T MANE Select	NP_660305.2:n.*7A>T
NR_026699.2:n.1669A>T
NR_026700.2:n.775A>T
NR_026701.2:n.1667A>T
NR_026702.2:n.705A>T
NM_001144951.2:c.*698A>T	NP_001138423.1:n.*698A>T