Canonical Allele Identifier: CA353076877

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293111-C-T
• MyVariant Identifiers: chr3:g.52327127C>T (hg19) ; chr3:g.52293111C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293111C>T , CM000665.2:g.52293111C>T	GRCh38
NC_000003.11:g.52327127C>T , CM000665.1:g.52327127C>T	GRCh37
NC_000003.10:g.52302167C>T	NCBI36
NG_023246.1:g.10292C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1557C>T MANE Select	ENSP00000389175.2:p.Phe519=
ENST00000436784.6:c.1557C>T	ENSP00000389175.2:p.Phe519=
ENST00000461183.5:c.829C>T	ENSP00000417264.1:p.Pro277Ser
ENST00000471180.5:c.700C>T	ENSP00000417526.1:p.Pro234Ser
ENST00000473032.5:c.595C>T	ENSP00000418951.1:p.Pro199Ser
ENST00000486393.5:c.*920C>T	ENSP00000419868.1:n.*920C>T
ENST00000489173.1:n.1851C>T
NM_145262.3:c.1557C>T	NP_660305.2:p.Phe519=
NR_026699.1:n.1655C>T
NR_026700.1:n.761C>T
NR_026701.1:n.1653C>T
NR_026702.1:n.691C>T
XM_005264878.2:c.*676C>T	XP_005264935.1:n.*676C>T
XR_245095.2:n.2808C>T
XM_017005730.1:c.1176C>T	XP_016861219.1:p.Phe392=
XM_024453351.1:c.1557C>T	XP_024309119.1:p.Phe519=
XM_024453352.1:c.*676C>T	XP_024309120.1:n.*676C>T
XR_001740022.2:n.3459C>T
XR_001740023.2:n.2983C>T
XR_245095.4:n.2809C>T
NM_145262.4:c.1557C>T MANE Select	NP_660305.2:p.Phe519=
NR_026699.2:n.1647C>T
NR_026700.2:n.753C>T
NR_026701.2:n.1645C>T
NR_026702.2:n.683C>T
NM_001144951.2:c.*676C>T	NP_001138423.1:n.*676C>T