Canonical Allele Identifier: CA353076730

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327102A>C (hg19) ; chr3:g.52293086A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293086A>C , CM000665.2:g.52293086A>C	GRCh38
NC_000003.11:g.52327102A>C , CM000665.1:g.52327102A>C	GRCh37
NC_000003.10:g.52302142A>C	NCBI36
NG_023246.1:g.10267A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1532A>C MANE Select	ENSP00000389175.2:p.Asn511Thr
ENST00000436784.6:c.1532A>C	ENSP00000389175.2:p.Asn511Thr
ENST00000461183.5:c.804A>C	ENSP00000417264.1:p.Gln268His
ENST00000471180.5:c.675A>C	ENSP00000417526.1:p.Gln225His
ENST00000473032.5:c.570A>C	ENSP00000418951.1:p.Gln190His
ENST00000486393.5:c.*895A>C	ENSP00000419868.1:n.*895A>C
ENST00000489173.1:n.1826A>C
NM_145262.3:c.1532A>C	NP_660305.2:p.Asn511Thr
NR_026699.1:n.1630A>C
NR_026700.1:n.736A>C
NR_026701.1:n.1628A>C
NR_026702.1:n.666A>C
XM_005264878.2:c.*651A>C	XP_005264935.1:n.*651A>C
XR_245095.2:n.2783A>C
XM_017005730.1:c.1151A>C	XP_016861219.1:p.Asn384Thr
XM_024453351.1:c.1532A>C	XP_024309119.1:p.Asn511Thr
XM_024453352.1:c.*651A>C	XP_024309120.1:n.*651A>C
XR_001740022.2:n.3434A>C
XR_001740023.2:n.2958A>C
XR_245095.4:n.2784A>C
NM_145262.4:c.1532A>C MANE Select	NP_660305.2:p.Asn511Thr
NR_026699.2:n.1622A>C
NR_026700.2:n.728A>C
NR_026701.2:n.1620A>C
NR_026702.2:n.658A>C
NM_001144951.2:c.*651A>C	NP_001138423.1:n.*651A>C