Canonical Allele Identifier: CA2573134442

Gene: GCKR

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27508073_27508074delinsCC , CM000664.2:g.27508073_27508074delinsCC	GRCh38
NC_000002.11:g.27730940_27730941delinsCC , CM000664.1:g.27730940_27730941delinsCC	GRCh37
NC_000002.10:g.27584444_27584445delinsCC	NCBI36
NG_028024.1:g.16235_16236delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264717.7:c.1337_1338delinsCC MANE Select	ENSP00000264717.2:p.Leu446Pro
ENST00000264717.6:c.1337_1338delinsCC	ENSP00000264717.2:p.Leu446Pro
ENST00000411584.1:c.439_440delinsCC
ENST00000478147.1:n.534_535delinsCC
NM_001486.3:c.1337_1338delinsCC	NP_001477.2:p.Leu446Pro
XM_011532761.1:c.1184_1185delinsCC	XP_011531063.1:p.Leu395Pro
XM_011532762.1:c.767_768delinsCC	XP_011531064.1:p.Leu256Pro
XM_017003796.1:c.767_768delinsCC	XP_016859285.1:p.Leu256Pro
XM_017003797.1:c.767_768delinsCC	XP_016859286.1:p.Leu256Pro
NM_001486.4:c.1337_1338delinsCC MANE Select	NP_001477.2:p.Leu446Pro