Canonical Allele Identifier: CA2665985217

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293328-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293328T>C , CM000665.2:g.52293328T>C	GRCh38
NC_000003.11:g.52327344T>C , CM000665.1:g.52327344T>C	GRCh37
NC_000003.10:g.52302384T>C	NCBI36
NG_023246.1:g.10509T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*202T>C MANE Select	ENSP00000389175.2:n.*202T>C
ENST00000436784.6:c.*202T>C	ENSP00000389175.2:n.*202T>C
ENST00000471180.5:c.*80T>C	ENSP00000417526.1:n.*80T>C
ENST00000473032.5:c.*80T>C	ENSP00000418951.1:n.*80T>C
ENST00000486393.5:c.*1137T>C	ENSP00000419868.1:n.*1137T>C
ENST00000489173.1:n.1936T>C
NM_145262.3:c.*202T>C	NP_660305.2:n.*202T>C
NR_026699.1:n.1872T>C
NR_026700.1:n.864T>C
NR_026701.1:n.1756T>C
NR_026702.1:n.794T>C
XM_005264878.2:c.*893T>C	XP_005264935.1:n.*893T>C
XR_245095.2:n.2911T>C
XM_017005730.1:c.*202T>C	XP_016861219.1:n.*202T>C
XM_024453351.1:c.*202T>C	XP_024309119.1:n.*202T>C
XM_024453352.1:c.*893T>C	XP_024309120.1:n.*893T>C
XR_001740022.2:n.3562T>C
XR_001740023.2:n.3086T>C
XR_245095.4:n.2912T>C
NM_145262.4:c.*202T>C MANE Select	NP_660305.2:n.*202T>C
NR_026699.2:n.1864T>C
NR_026700.2:n.856T>C
NR_026701.2:n.1748T>C
NR_026702.2:n.786T>C
NM_001144951.2:c.*893T>C	NP_001138423.1:n.*893T>C