Canonical Allele Identifier: CA1240316023
Gene: GCKR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27519758_27519759delinsAT , CM000664.2:g.27519758_27519759delinsAT GRCh38
NC_000002.11:g.27742625_27742626delinsAT , CM000664.1:g.27742625_27742626delinsAT GRCh37
NC_000002.10:g.27596129_27596130delinsAT NCBI36
NG_028024.1:g.27920_27921delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000264717.7:c.1572+821_1572+822delinsAT MANE Select ENSP00000264717.2:n.1572+821_1572+822deli...
ENST00000264717.6:c.1572+821_1572+822delinsAT ENSP00000264717.2:n.1572+821_1572+822deli...
NM_001486.3:c.1572+821_1572+822delinsAT NP_001477.2:n.1572+821_1572+822delinsAT
XM_011532761.1:c.1419+821_1419+822delinsAT XP_011531063.1:n.1419+821_1419+822delinsA...
XM_011532762.1:c.1002+821_1002+822delinsAT XP_011531064.1:n.1002+821_1002+822delinsA...
XM_017003796.1:c.1002+821_1002+822delinsAT XP_016859285.1:n.1002+821_1002+822delinsA...
XM_017003797.1:c.1002+821_1002+822delinsAT XP_016859286.1:n.1002+821_1002+822delinsA...
NM_001486.4:c.1572+821_1572+822delinsAT MANE Select NP_001477.2:n.1572+821_1572+822delinsAT
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