Canonical Allele Identifier: CA2838202636

Gene: GCKR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27522416dup , CM000664.2:g.27522416dup	GRCh38
NC_000002.11:g.27745283dup , CM000664.1:g.27745283dup	GRCh37
NC_000002.10:g.27598787dup	NCBI36
NG_028024.1:g.30578dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264717.7:c.1573-44dup MANE Select	ENSP00000264717.2:n.1573-44dup
ENST00000264717.6:c.1573-44dup	ENSP00000264717.2:n.1573-44dup
NM_001486.3:c.1573-44dup	NP_001477.2:n.1573-44dup
XM_011532761.1:c.1420-44dup	XP_011531063.1:n.1420-44dup
XM_011532762.1:c.1003-44dup	XP_011531064.1:n.1003-44dup
XM_017003796.1:c.1003-44dup	XP_016859285.1:n.1003-44dup
XM_017003797.1:c.1003-44dup	XP_016859286.1:n.1003-44dup
NM_001486.4:c.1573-44dup MANE Select	NP_001477.2:n.1573-44dup