Canonical Allele Identifier: CA1240316022
Gene: GCKR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27519758A= , CM000664.2:g.27519758A= GRCh38
NC_000002.11:g.27742625A= , CM000664.1:g.27742625A= GRCh37
NC_000002.10:g.27596129A= NCBI36
NG_028024.1:g.27920A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264717.7:c.1572+821A= MANE Select ENSP00000264717.2:n.1572+821A=
ENST00000264717.6:c.1572+821A= ENSP00000264717.2:n.1572+821A=
NM_001486.3:c.1572+821A= NP_001477.2:n.1572+821A=
XM_011532761.1:c.1419+821A= XP_011531063.1:n.1419+821A=
XM_011532762.1:c.1002+821A= XP_011531064.1:n.1002+821A=
XM_017003796.1:c.1002+821A= XP_016859285.1:n.1002+821A=
XM_017003797.1:c.1002+821A= XP_016859286.1:n.1002+821A=
NM_001486.4:c.1572+821A= MANE Select NP_001477.2:n.1572+821A=
Search 100 bp 5'
Search 100 bp 3'