Canonical Allele Identifier: CA1240316013
Gene: GCKR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27519737G= , CM000664.2:g.27519737G= GRCh38
NC_000002.11:g.27742604G= , CM000664.1:g.27742604G= GRCh37
NC_000002.10:g.27596108G= NCBI36
NG_028024.1:g.27899G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264717.7:c.1572+800G= MANE Select ENSP00000264717.2:n.1572+800G=
ENST00000264717.6:c.1572+800G= ENSP00000264717.2:n.1572+800G=
NM_001486.3:c.1572+800G= NP_001477.2:n.1572+800G=
XM_011532761.1:c.1419+800G= XP_011531063.1:n.1419+800G=
XM_011532762.1:c.1002+800G= XP_011531064.1:n.1002+800G=
XM_017003796.1:c.1002+800G= XP_016859285.1:n.1002+800G=
XM_017003797.1:c.1002+800G= XP_016859286.1:n.1002+800G=
NM_001486.4:c.1572+800G= MANE Select NP_001477.2:n.1572+800G=
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