Canonical Allele Identifier: CA353076778

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327111A>C (hg19) ; chr3:g.52293095A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293095A>C , CM000665.2:g.52293095A>C	GRCh38
NC_000003.11:g.52327111A>C , CM000665.1:g.52327111A>C	GRCh37
NC_000003.10:g.52302151A>C	NCBI36
NG_023246.1:g.10276A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1541A>C MANE Select	ENSP00000389175.2:p.Asp514Ala
ENST00000436784.6:c.1541A>C	ENSP00000389175.2:p.Asp514Ala
ENST00000461183.5:c.813A>C	ENSP00000417264.1:p.Gly271=
ENST00000471180.5:c.684A>C	ENSP00000417526.1:p.Gly228=
ENST00000473032.5:c.579A>C	ENSP00000418951.1:p.Gly193=
ENST00000486393.5:c.*904A>C	ENSP00000419868.1:n.*904A>C
ENST00000489173.1:n.1835A>C
NM_145262.3:c.1541A>C	NP_660305.2:p.Asp514Ala
NR_026699.1:n.1639A>C
NR_026700.1:n.745A>C
NR_026701.1:n.1637A>C
NR_026702.1:n.675A>C
XM_005264878.2:c.*660A>C	XP_005264935.1:n.*660A>C
XR_245095.2:n.2792A>C
XM_017005730.1:c.1160A>C	XP_016861219.1:p.Asp387Ala
XM_024453351.1:c.1541A>C	XP_024309119.1:p.Asp514Ala
XM_024453352.1:c.*660A>C	XP_024309120.1:n.*660A>C
XR_001740022.2:n.3443A>C
XR_001740023.2:n.2967A>C
XR_245095.4:n.2793A>C
NM_145262.4:c.1541A>C MANE Select	NP_660305.2:p.Asp514Ala
NR_026699.2:n.1631A>C
NR_026700.2:n.737A>C
NR_026701.2:n.1629A>C
NR_026702.2:n.667A>C
NM_001144951.2:c.*660A>C	NP_001138423.1:n.*660A>C