Canonical Allele Identifier: CA433882939

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326950T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292934T>C , CM000665.2:g.52292934T>C	GRCh38
NC_000003.11:g.52326950T>C , CM000665.1:g.52326950T>C	GRCh37
NC_000003.10:g.52301990T>C	NCBI36
NG_023246.1:g.10115T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1380T>C MANE Select	ENSP00000389175.2:p.Ala460=
ENST00000305690.12:c.*499T>C	ENSP00000301965.9:n.*499T>C
ENST00000436784.6:c.1380T>C	ENSP00000389175.2:p.Ala460=
ENST00000461183.5:c.764-112T>C	ENSP00000417264.1:n.764-112T>C
ENST00000471180.5:c.635-112T>C	ENSP00000417526.1:n.635-112T>C
ENST00000473032.5:c.530-112T>C	ENSP00000418951.1:n.530-112T>C
ENST00000477382.1:c.*499T>C	ENSP00000419008.1:n.*499T>C
ENST00000486393.5:c.*743T>C	ENSP00000419868.1:n.*743T>C
ENST00000489173.1:n.1674T>C
NM_001144951.1:c.*499T>C	NP_001138423.1:n.*499T>C
NM_145262.3:c.1380T>C	NP_660305.2:p.Ala460=
NR_026699.1:n.1478T>C
NR_026700.1:n.696-112T>C
NR_026701.1:n.1476T>C
NR_026702.1:n.626-112T>C
XM_005264878.2:c.*499T>C	XP_005264935.1:n.*499T>C
XR_245095.2:n.2743-112T>C
XM_017005730.1:c.999T>C	XP_016861219.1:p.Ala333=
XM_024453351.1:c.1380T>C	XP_024309119.1:p.Ala460=
XM_024453352.1:c.*499T>C	XP_024309120.1:n.*499T>C
XR_001740022.2:n.3282T>C
XR_001740023.2:n.2918-112T>C
XR_245095.4:n.2744-112T>C
NM_145262.4:c.1380T>C MANE Select	NP_660305.2:p.Ala460=
NR_026699.2:n.1470T>C
NR_026700.2:n.688-112T>C
NR_026701.2:n.1468T>C
NR_026702.2:n.618-112T>C
NM_001144951.2:c.*499T>C	NP_001138423.1:n.*499T>C