Canonical Allele Identifier: CA1364789272
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52293140_52293141delinsAT , CM000665.2:g.52293140_52293141delinsAT GRCh38
NC_000003.11:g.52327156_52327157delinsAT , CM000665.1:g.52327156_52327157delinsAT GRCh37
NC_000003.10:g.52302196_52302197delinsAT NCBI36
NG_023246.1:g.10321_10322delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000436784.7:c.*14_*15delinsAT MANE Select ENSP00000389175.2:n.*14_*15delinsAT
ENST00000436784.6:c.*14_*15delinsAT ENSP00000389175.2:n.*14_*15delinsAT
ENST00000461183.5:c.*6_*7delinsAT ENSP00000417264.1:n.*6_*7delinsAT
ENST00000471180.5:c.*6_*7delinsAT ENSP00000417526.1:n.*6_*7delinsAT
ENST00000473032.5:c.*6_*7delinsAT ENSP00000418951.1:n.*6_*7delinsAT
ENST00000486393.5:c.*949_*950delinsAT ENSP00000419868.1:n.*949_*950delinsAT
ENST00000489173.1:n.1880_1881delinsAT
NM_145262.3:c.*14_*15delinsAT NP_660305.2:n.*14_*15delinsAT
NR_026699.1:n.1684_1685delinsAT
NR_026700.1:n.790_791delinsAT
NR_026701.1:n.1682_1683delinsAT
NR_026702.1:n.720_721delinsAT
XM_005264878.2:c.*705_*706delinsAT XP_005264935.1:n.*705_*706delinsAT
XR_245095.2:n.2837_2838delinsAT
XM_017005730.1:c.*14_*15delinsAT XP_016861219.1:n.*14_*15delinsAT
XM_024453351.1:c.*14_*15delinsAT XP_024309119.1:n.*14_*15delinsAT
XM_024453352.1:c.*705_*706delinsAT XP_024309120.1:n.*705_*706delinsAT
XR_001740022.2:n.3488_3489delinsAT
XR_001740023.2:n.3012_3013delinsAT
XR_245095.4:n.2838_2839delinsAT
NM_145262.4:c.*14_*15delinsAT MANE Select NP_660305.2:n.*14_*15delinsAT
NR_026699.2:n.1676_1677delinsAT
NR_026700.2:n.782_783delinsAT
NR_026701.2:n.1674_1675delinsAT
NR_026702.2:n.712_713delinsAT
NM_001144951.2:c.*705_*706delinsAT NP_001138423.1:n.*705_*706delinsAT