Canonical Allele Identifier: CA433883018

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327004G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292988G>C , CM000665.2:g.52292988G>C	GRCh38
NC_000003.11:g.52327004G>C , CM000665.1:g.52327004G>C	GRCh37
NC_000003.10:g.52302044G>C	NCBI36
NG_023246.1:g.10169G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1434G>C MANE Select	ENSP00000389175.2:p.Leu478=
ENST00000305690.12:c.*553G>C	ENSP00000301965.9:n.*553G>C
ENST00000436784.6:c.1434G>C	ENSP00000389175.2:p.Leu478=
ENST00000461183.5:c.764-58G>C	ENSP00000417264.1:n.764-58G>C
ENST00000471180.5:c.635-58G>C	ENSP00000417526.1:n.635-58G>C
ENST00000473032.5:c.530-58G>C	ENSP00000418951.1:n.530-58G>C
ENST00000477382.1:c.*553G>C	ENSP00000419008.1:n.*553G>C
ENST00000486393.5:c.*797G>C	ENSP00000419868.1:n.*797G>C
ENST00000489173.1:n.1728G>C
NM_001144951.1:c.*553G>C	NP_001138423.1:n.*553G>C
NM_145262.3:c.1434G>C	NP_660305.2:p.Leu478=
NR_026699.1:n.1532G>C
NR_026700.1:n.696-58G>C
NR_026701.1:n.1530G>C
NR_026702.1:n.626-58G>C
XM_005264878.2:c.*553G>C	XP_005264935.1:n.*553G>C
XR_245095.2:n.2743-58G>C
XM_017005730.1:c.1053G>C	XP_016861219.1:p.Leu351=
XM_024453351.1:c.1434G>C	XP_024309119.1:p.Leu478=
XM_024453352.1:c.*553G>C	XP_024309120.1:n.*553G>C
XR_001740022.2:n.3336G>C
XR_001740023.2:n.2918-58G>C
XR_245095.4:n.2744-58G>C
NM_145262.4:c.1434G>C MANE Select	NP_660305.2:p.Leu478=
NR_026699.2:n.1524G>C
NR_026700.2:n.688-58G>C
NR_026701.2:n.1522G>C
NR_026702.2:n.618-58G>C
NM_001144951.2:c.*553G>C	NP_001138423.1:n.*553G>C