Canonical Allele Identifier: CA433752113

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327174A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293158A>C , CM000665.2:g.52293158A>C	GRCh38
NC_000003.11:g.52327174A>C , CM000665.1:g.52327174A>C	GRCh37
NC_000003.10:g.52302214A>C	NCBI36
NG_023246.1:g.10339A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*32A>C MANE Select	ENSP00000389175.2:n.*32A>C
ENST00000436784.6:c.*32A>C	ENSP00000389175.2:n.*32A>C
ENST00000461183.5:c.*24A>C	ENSP00000417264.1:n.*24A>C
ENST00000471180.5:c.*24A>C	ENSP00000417526.1:n.*24A>C
ENST00000473032.5:c.*24A>C	ENSP00000418951.1:n.*24A>C
ENST00000486393.5:c.*967A>C	ENSP00000419868.1:n.*967A>C
ENST00000489173.1:n.1898A>C
NM_145262.3:c.*32A>C	NP_660305.2:n.*32A>C
NR_026699.1:n.1702A>C
NR_026700.1:n.808A>C
NR_026701.1:n.1700A>C
NR_026702.1:n.738A>C
XM_005264878.2:c.*723A>C	XP_005264935.1:n.*723A>C
XR_245095.2:n.2855A>C
XM_017005730.1:c.*32A>C	XP_016861219.1:n.*32A>C
XM_024453351.1:c.*32A>C	XP_024309119.1:n.*32A>C
XM_024453352.1:c.*723A>C	XP_024309120.1:n.*723A>C
XR_001740022.2:n.3506A>C
XR_001740023.2:n.3030A>C
XR_245095.4:n.2856A>C
NM_145262.4:c.*32A>C MANE Select	NP_660305.2:n.*32A>C
NR_026699.2:n.1694A>C
NR_026700.2:n.800A>C
NR_026701.2:n.1692A>C
NR_026702.2:n.730A>C
NM_001144951.2:c.*723A>C	NP_001138423.1:n.*723A>C