Canonical Allele Identifier: CA353076728

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327101A>C (hg19) ; chr3:g.52293085A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293085A>C , CM000665.2:g.52293085A>C	GRCh38
NC_000003.11:g.52327101A>C , CM000665.1:g.52327101A>C	GRCh37
NC_000003.10:g.52302141A>C	NCBI36
NG_023246.1:g.10266A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1531A>C MANE Select	ENSP00000389175.2:p.Asn511His
ENST00000436784.6:c.1531A>C	ENSP00000389175.2:p.Asn511His
ENST00000461183.5:c.803A>C	ENSP00000417264.1:p.Gln268Pro
ENST00000471180.5:c.674A>C	ENSP00000417526.1:p.Gln225Pro
ENST00000473032.5:c.569A>C	ENSP00000418951.1:p.Gln190Pro
ENST00000486393.5:c.*894A>C	ENSP00000419868.1:n.*894A>C
ENST00000489173.1:n.1825A>C
NM_145262.3:c.1531A>C	NP_660305.2:p.Asn511His
NR_026699.1:n.1629A>C
NR_026700.1:n.735A>C
NR_026701.1:n.1627A>C
NR_026702.1:n.665A>C
XM_005264878.2:c.*650A>C	XP_005264935.1:n.*650A>C
XR_245095.2:n.2782A>C
XM_017005730.1:c.1150A>C	XP_016861219.1:p.Asn384His
XM_024453351.1:c.1531A>C	XP_024309119.1:p.Asn511His
XM_024453352.1:c.*650A>C	XP_024309120.1:n.*650A>C
XR_001740022.2:n.3433A>C
XR_001740023.2:n.2957A>C
XR_245095.4:n.2783A>C
NM_145262.4:c.1531A>C MANE Select	NP_660305.2:p.Asn511His
NR_026699.2:n.1621A>C
NR_026700.2:n.727A>C
NR_026701.2:n.1619A>C
NR_026702.2:n.657A>C
NM_001144951.2:c.*650A>C	NP_001138423.1:n.*650A>C