Canonical Allele Identifier: CA353076675

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327091G>C (hg19) ; chr3:g.52293075G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293075G>C , CM000665.2:g.52293075G>C	GRCh38
NC_000003.11:g.52327091G>C , CM000665.1:g.52327091G>C	GRCh37
NC_000003.10:g.52302131G>C	NCBI36
NG_023246.1:g.10256G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1521G>C MANE Select	ENSP00000389175.2:p.Met507Ile
ENST00000436784.6:c.1521G>C	ENSP00000389175.2:p.Met507Ile
ENST00000461183.5:c.793G>C	ENSP00000417264.1:p.Asp265His
ENST00000471180.5:c.664G>C	ENSP00000417526.1:p.Asp222His
ENST00000473032.5:c.559G>C	ENSP00000418951.1:p.Asp187His
ENST00000486393.5:c.*884G>C	ENSP00000419868.1:n.*884G>C
ENST00000489173.1:n.1815G>C
NM_145262.3:c.1521G>C	NP_660305.2:p.Met507Ile
NR_026699.1:n.1619G>C
NR_026700.1:n.725G>C
NR_026701.1:n.1617G>C
NR_026702.1:n.655G>C
XM_005264878.2:c.*640G>C	XP_005264935.1:n.*640G>C
XR_245095.2:n.2772G>C
XM_017005730.1:c.1140G>C	XP_016861219.1:p.Met380Ile
XM_024453351.1:c.1521G>C	XP_024309119.1:p.Met507Ile
XM_024453352.1:c.*640G>C	XP_024309120.1:n.*640G>C
XR_001740022.2:n.3423G>C
XR_001740023.2:n.2947G>C
XR_245095.4:n.2773G>C
NM_145262.4:c.1521G>C MANE Select	NP_660305.2:p.Met507Ile
NR_026699.2:n.1611G>C
NR_026700.2:n.717G>C
NR_026701.2:n.1609G>C
NR_026702.2:n.647G>C
NM_001144951.2:c.*640G>C	NP_001138423.1:n.*640G>C