Canonical Allele Identifier: CA2838229383

Gene: GCKR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27506973A>T , CM000664.2:g.27506973A>T	GRCh38
NC_000002.11:g.27729840A>T , CM000664.1:g.27729840A>T	GRCh37
NC_000002.10:g.27583344A>T	NCBI36
NG_028024.1:g.15135A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264717.7:c.1066+88A>T MANE Select	ENSP00000264717.2:n.1066+88A>T
ENST00000264717.6:c.1066+88A>T	ENSP00000264717.2:n.1066+88A>T
ENST00000411584.1:c.168+88A>T
NM_001486.3:c.1066+88A>T	NP_001477.2:n.1066+88A>T
XM_011532761.1:c.990+372A>T	XP_011531063.1:n.990+372A>T
XM_011532762.1:c.496+88A>T	XP_011531064.1:n.496+88A>T
XM_011532763.1:c.969-262A>T	XP_011531065.1:n.969-262A>T
XM_017003796.1:c.496+88A>T	XP_016859285.1:n.496+88A>T
XM_017003797.1:c.496+88A>T	XP_016859286.1:n.496+88A>T
XR_001738699.1:n.1034+394A>T
NM_001486.4:c.1066+88A>T MANE Select	NP_001477.2:n.1066+88A>T