Canonical Allele Identifier: CA353076624

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327081A>C (hg19) ; chr3:g.52293065A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293065A>C , CM000665.2:g.52293065A>C	GRCh38
NC_000003.11:g.52327081A>C , CM000665.1:g.52327081A>C	GRCh37
NC_000003.10:g.52302121A>C	NCBI36
NG_023246.1:g.10246A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1511A>C MANE Select	ENSP00000389175.2:p.His504Pro
ENST00000436784.6:c.1511A>C	ENSP00000389175.2:p.His504Pro
ENST00000461183.5:c.783A>C	ENSP00000417264.1:p.Ala261=
ENST00000471180.5:c.654A>C	ENSP00000417526.1:p.Ala218=
ENST00000473032.5:c.549A>C	ENSP00000418951.1:p.Ala183=
ENST00000486393.5:c.*874A>C	ENSP00000419868.1:n.*874A>C
ENST00000489173.1:n.1805A>C
NM_145262.3:c.1511A>C	NP_660305.2:p.His504Pro
NR_026699.1:n.1609A>C
NR_026700.1:n.715A>C
NR_026701.1:n.1607A>C
NR_026702.1:n.645A>C
XM_005264878.2:c.*630A>C	XP_005264935.1:n.*630A>C
XR_245095.2:n.2762A>C
XM_017005730.1:c.1130A>C	XP_016861219.1:p.His377Pro
XM_024453351.1:c.1511A>C	XP_024309119.1:p.His504Pro
XM_024453352.1:c.*630A>C	XP_024309120.1:n.*630A>C
XR_001740022.2:n.3413A>C
XR_001740023.2:n.2937A>C
XR_245095.4:n.2763A>C
NM_145262.4:c.1511A>C MANE Select	NP_660305.2:p.His504Pro
NR_026699.2:n.1601A>C
NR_026700.2:n.707A>C
NR_026701.2:n.1599A>C
NR_026702.2:n.637A>C
NM_001144951.2:c.*630A>C	NP_001138423.1:n.*630A>C