Canonical Allele Identifier: CA353076614

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327077C>T (hg19) ; chr3:g.52293061C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293061C>T , CM000665.2:g.52293061C>T	GRCh38
NC_000003.11:g.52327077C>T , CM000665.1:g.52327077C>T	GRCh37
NC_000003.10:g.52302117C>T	NCBI36
NG_023246.1:g.10242C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1507C>T MANE Select	ENSP00000389175.2:p.Leu503=
ENST00000436784.6:c.1507C>T	ENSP00000389175.2:p.Leu503=
ENST00000461183.5:c.779C>T	ENSP00000417264.1:p.Ala260Val
ENST00000471180.5:c.650C>T	ENSP00000417526.1:p.Ala217Val
ENST00000473032.5:c.545C>T	ENSP00000418951.1:p.Ala182Val
ENST00000486393.5:c.*870C>T	ENSP00000419868.1:n.*870C>T
ENST00000489173.1:n.1801C>T
NM_145262.3:c.1507C>T	NP_660305.2:p.Leu503=
NR_026699.1:n.1605C>T
NR_026700.1:n.711C>T
NR_026701.1:n.1603C>T
NR_026702.1:n.641C>T
XM_005264878.2:c.*626C>T	XP_005264935.1:n.*626C>T
XR_245095.2:n.2758C>T
XM_017005730.1:c.1126C>T	XP_016861219.1:p.Leu376=
XM_024453351.1:c.1507C>T	XP_024309119.1:p.Leu503=
XM_024453352.1:c.*626C>T	XP_024309120.1:n.*626C>T
XR_001740022.2:n.3409C>T
XR_001740023.2:n.2933C>T
XR_245095.4:n.2759C>T
NM_145262.4:c.1507C>T MANE Select	NP_660305.2:p.Leu503=
NR_026699.2:n.1597C>T
NR_026700.2:n.703C>T
NR_026701.2:n.1595C>T
NR_026702.2:n.633C>T
NM_001144951.2:c.*626C>T	NP_001138423.1:n.*626C>T