Canonical Allele Identifier: CA2665985216

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293327-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293327T>C , CM000665.2:g.52293327T>C	GRCh38
NC_000003.11:g.52327343T>C , CM000665.1:g.52327343T>C	GRCh37
NC_000003.10:g.52302383T>C	NCBI36
NG_023246.1:g.10508T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*201T>C MANE Select	ENSP00000389175.2:n.*201T>C
ENST00000436784.6:c.*201T>C	ENSP00000389175.2:n.*201T>C
ENST00000471180.5:c.*79T>C	ENSP00000417526.1:n.*79T>C
ENST00000473032.5:c.*79T>C	ENSP00000418951.1:n.*79T>C
ENST00000486393.5:c.*1136T>C	ENSP00000419868.1:n.*1136T>C
ENST00000489173.1:n.1935T>C
NM_145262.3:c.*201T>C	NP_660305.2:n.*201T>C
NR_026699.1:n.1871T>C
NR_026700.1:n.863T>C
NR_026701.1:n.1755T>C
NR_026702.1:n.793T>C
XM_005264878.2:c.*892T>C	XP_005264935.1:n.*892T>C
XR_245095.2:n.2910T>C
XM_017005730.1:c.*201T>C	XP_016861219.1:n.*201T>C
XM_024453351.1:c.*201T>C	XP_024309119.1:n.*201T>C
XM_024453352.1:c.*892T>C	XP_024309120.1:n.*892T>C
XR_001740022.2:n.3561T>C
XR_001740023.2:n.3085T>C
XR_245095.4:n.2911T>C
NM_145262.4:c.*201T>C MANE Select	NP_660305.2:n.*201T>C
NR_026699.2:n.1863T>C
NR_026700.2:n.855T>C
NR_026701.2:n.1747T>C
NR_026702.2:n.785T>C
NM_001144951.2:c.*892T>C	NP_001138423.1:n.*892T>C