Canonical Allele Identifier: CA353075742

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326878G>C (hg19) ; chr3:g.52292862G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292862G>C , CM000665.2:g.52292862G>C	GRCh38
NC_000003.11:g.52326878G>C , CM000665.1:g.52326878G>C	GRCh37
NC_000003.10:g.52301918G>C	NCBI36
NG_023246.1:g.10043G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1308G>C MANE Select	ENSP00000389175.2:p.Arg436Ser
ENST00000305690.12:c.*427G>C	ENSP00000301965.9:n.*427G>C
ENST00000436784.6:c.1308G>C	ENSP00000389175.2:p.Arg436Ser
ENST00000461183.5:c.764-184G>C	ENSP00000417264.1:n.764-184G>C
ENST00000471180.5:c.635-184G>C	ENSP00000417526.1:n.635-184G>C
ENST00000473032.5:c.530-184G>C	ENSP00000418951.1:n.530-184G>C
ENST00000477382.1:c.*427G>C	ENSP00000419008.1:n.*427G>C
ENST00000486393.5:c.*671G>C	ENSP00000419868.1:n.*671G>C
ENST00000489173.1:n.1602G>C
NM_001144951.1:c.*427G>C	NP_001138423.1:n.*427G>C
NM_145262.3:c.1308G>C	NP_660305.2:p.Arg436Ser
NR_026699.1:n.1406G>C
NR_026700.1:n.696-184G>C
NR_026701.1:n.1404G>C
NR_026702.1:n.626-184G>C
XM_005264878.2:c.*427G>C	XP_005264935.1:n.*427G>C
XR_245095.2:n.2743-184G>C
XM_017005730.1:c.927G>C	XP_016861219.1:p.Arg309Ser
XM_024453351.1:c.1308G>C	XP_024309119.1:p.Arg436Ser
XM_024453352.1:c.*427G>C	XP_024309120.1:n.*427G>C
XR_001740022.2:n.3210G>C
XR_001740023.2:n.2918-184G>C
XR_245095.4:n.2744-184G>C
NM_145262.4:c.1308G>C MANE Select	NP_660305.2:p.Arg436Ser
NR_026699.2:n.1398G>C
NR_026700.2:n.688-184G>C
NR_026701.2:n.1396G>C
NR_026702.2:n.618-184G>C
NM_001144951.2:c.*427G>C	NP_001138423.1:n.*427G>C