Canonical Allele Identifier: CA433752041

Gene: GLYCTK

Linked Data

• dbSNP Id: rs758280911
• MyVariant Identifiers: chr3:g.52327085A>C (hg19) ; chr3:g.52293069A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293069A>C , CM000665.2:g.52293069A>C	GRCh38
NC_000003.11:g.52327085A>C , CM000665.1:g.52327085A>C	GRCh37
NC_000003.10:g.52302125A>C	NCBI36
NG_023246.1:g.10250A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1515A>C MANE Select	ENSP00000389175.2:p.Thr505=
ENST00000436784.6:c.1515A>C	ENSP00000389175.2:p.Thr505=
ENST00000461183.5:c.787A>C	ENSP00000417264.1:p.Arg263=
ENST00000471180.5:c.658A>C	ENSP00000417526.1:p.Arg220=
ENST00000473032.5:c.553A>C	ENSP00000418951.1:p.Arg185=
ENST00000486393.5:c.*878A>C	ENSP00000419868.1:n.*878A>C
ENST00000489173.1:n.1809A>C
NM_145262.3:c.1515A>C	NP_660305.2:p.Thr505=
NR_026699.1:n.1613A>C
NR_026700.1:n.719A>C
NR_026701.1:n.1611A>C
NR_026702.1:n.649A>C
XM_005264878.2:c.*634A>C	XP_005264935.1:n.*634A>C
XR_245095.2:n.2766A>C
XM_017005730.1:c.1134A>C	XP_016861219.1:p.Thr378=
XM_024453351.1:c.1515A>C	XP_024309119.1:p.Thr505=
XM_024453352.1:c.*634A>C	XP_024309120.1:n.*634A>C
XR_001740022.2:n.3417A>C
XR_001740023.2:n.2941A>C
XR_245095.4:n.2767A>C
NM_145262.4:c.1515A>C MANE Select	NP_660305.2:p.Thr505=
NR_026699.2:n.1605A>C
NR_026700.2:n.711A>C
NR_026701.2:n.1603A>C
NR_026702.2:n.641A>C
NM_001144951.2:c.*634A>C	NP_001138423.1:n.*634A>C