Canonical Allele Identifier: CA353076092

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326964T>C (hg19) ; chr3:g.52292948T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292948T>C , CM000665.2:g.52292948T>C	GRCh38
NC_000003.11:g.52326964T>C , CM000665.1:g.52326964T>C	GRCh37
NC_000003.10:g.52302004T>C	NCBI36
NG_023246.1:g.10129T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1394T>C MANE Select	ENSP00000389175.2:p.Val465Ala
ENST00000305690.12:c.*513T>C	ENSP00000301965.9:n.*513T>C
ENST00000436784.6:c.1394T>C	ENSP00000389175.2:p.Val465Ala
ENST00000461183.5:c.764-98T>C	ENSP00000417264.1:n.764-98T>C
ENST00000471180.5:c.635-98T>C	ENSP00000417526.1:n.635-98T>C
ENST00000473032.5:c.530-98T>C	ENSP00000418951.1:n.530-98T>C
ENST00000477382.1:c.*513T>C	ENSP00000419008.1:n.*513T>C
ENST00000486393.5:c.*757T>C	ENSP00000419868.1:n.*757T>C
ENST00000489173.1:n.1688T>C
NM_001144951.1:c.*513T>C	NP_001138423.1:n.*513T>C
NM_145262.3:c.1394T>C	NP_660305.2:p.Val465Ala
NR_026699.1:n.1492T>C
NR_026700.1:n.696-98T>C
NR_026701.1:n.1490T>C
NR_026702.1:n.626-98T>C
XM_005264878.2:c.*513T>C	XP_005264935.1:n.*513T>C
XR_245095.2:n.2743-98T>C
XM_017005730.1:c.1013T>C	XP_016861219.1:p.Val338Ala
XM_024453351.1:c.1394T>C	XP_024309119.1:p.Val465Ala
XM_024453352.1:c.*513T>C	XP_024309120.1:n.*513T>C
XR_001740022.2:n.3296T>C
XR_001740023.2:n.2918-98T>C
XR_245095.4:n.2744-98T>C
NM_145262.4:c.1394T>C MANE Select	NP_660305.2:p.Val465Ala
NR_026699.2:n.1484T>C
NR_026700.2:n.688-98T>C
NR_026701.2:n.1482T>C
NR_026702.2:n.618-98T>C
NM_001144951.2:c.*513T>C	NP_001138423.1:n.*513T>C