Canonical Allele Identifier: CA353076929

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327136T>G (hg19) ; chr3:g.52293120T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293120T>G , CM000665.2:g.52293120T>G	GRCh38
NC_000003.11:g.52327136T>G , CM000665.1:g.52327136T>G	GRCh37
NC_000003.10:g.52302176T>G	NCBI36
NG_023246.1:g.10301T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1566T>G MANE Select	ENSP00000389175.2:p.Pro522=
ENST00000436784.6:c.1566T>G	ENSP00000389175.2:p.Pro522=
ENST00000461183.5:c.838T>G	ENSP00000417264.1:p.Ser280Ala
ENST00000471180.5:c.709T>G	ENSP00000417526.1:p.Ser237Ala
ENST00000473032.5:c.604T>G	ENSP00000418951.1:p.Ser202Ala
ENST00000486393.5:c.*929T>G	ENSP00000419868.1:n.*929T>G
ENST00000489173.1:n.1860T>G
NM_145262.3:c.1566T>G	NP_660305.2:p.Pro522=
NR_026699.1:n.1664T>G
NR_026700.1:n.770T>G
NR_026701.1:n.1662T>G
NR_026702.1:n.700T>G
XM_005264878.2:c.*685T>G	XP_005264935.1:n.*685T>G
XR_245095.2:n.2817T>G
XM_017005730.1:c.1185T>G	XP_016861219.1:p.Pro395=
XM_024453351.1:c.1566T>G	XP_024309119.1:p.Pro522=
XM_024453352.1:c.*685T>G	XP_024309120.1:n.*685T>G
XR_001740022.2:n.3468T>G
XR_001740023.2:n.2992T>G
XR_245095.4:n.2818T>G
NM_145262.4:c.1566T>G MANE Select	NP_660305.2:p.Pro522=
NR_026699.2:n.1656T>G
NR_026700.2:n.762T>G
NR_026701.2:n.1654T>G
NR_026702.2:n.692T>G
NM_001144951.2:c.*685T>G	NP_001138423.1:n.*685T>G