Canonical Allele Identifier: CA433752059

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327154A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293138A>T , CM000665.2:g.52293138A>T	GRCh38
NC_000003.11:g.52327154A>T , CM000665.1:g.52327154A>T	GRCh37
NC_000003.10:g.52302194A>T	NCBI36
NG_023246.1:g.10319A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*12A>T MANE Select	ENSP00000389175.2:n.*12A>T
ENST00000436784.6:c.*12A>T	ENSP00000389175.2:n.*12A>T
ENST00000461183.5:c.*4A>T	ENSP00000417264.1:n.*4A>T
ENST00000471180.5:c.*4A>T	ENSP00000417526.1:n.*4A>T
ENST00000473032.5:c.*4A>T	ENSP00000418951.1:n.*4A>T
ENST00000486393.5:c.*947A>T	ENSP00000419868.1:n.*947A>T
ENST00000489173.1:n.1878A>T
NM_145262.3:c.*12A>T	NP_660305.2:n.*12A>T
NR_026699.1:n.1682A>T
NR_026700.1:n.788A>T
NR_026701.1:n.1680A>T
NR_026702.1:n.718A>T
XM_005264878.2:c.*703A>T	XP_005264935.1:n.*703A>T
XR_245095.2:n.2835A>T
XM_017005730.1:c.*12A>T	XP_016861219.1:n.*12A>T
XM_024453351.1:c.*12A>T	XP_024309119.1:n.*12A>T
XM_024453352.1:c.*703A>T	XP_024309120.1:n.*703A>T
XR_001740022.2:n.3486A>T
XR_001740023.2:n.3010A>T
XR_245095.4:n.2836A>T
NM_145262.4:c.*12A>T MANE Select	NP_660305.2:n.*12A>T
NR_026699.2:n.1674A>T
NR_026700.2:n.780A>T
NR_026701.2:n.1672A>T
NR_026702.2:n.710A>T
NM_001144951.2:c.*703A>T	NP_001138423.1:n.*703A>T