Canonical Allele Identifier: CA1216113329

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122103_193122106delinsAAGG , CM000663.2:g.193122103_193122106delinsAAGG	GRCh38
NC_000001.10:g.193091233_193091236delinsAAGG , CM000663.1:g.193091233_193091236delinsAAGG	GRCh37
NC_000001.9:g.191357856_191357859delinsAAGG	NCBI36
NG_012691.1:g.5146_5149delinsAAGG , LRG_507:g.5146_5149delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-98_-95delinsAAGG MANE Select	ENSP00000356405.4:n.-98_-95delinsAAGG
ENST00000643006.1:c.-98_-95delinsAAGG	ENSP00000496633.1:n.-98_-95delinsAAGG
ENST00000649895.1:n.121_124delinsAAGG
ENST00000650197.1:c.-98_-95delinsAAGG	ENSP00000496929.1:n.-98_-95delinsAAGG
ENST00000367435.3:c.-98_-95delinsAAGG	ENSP00000356405.3:n.-98_-95delinsAAGG
NM_024529.4:c.-98_-95delinsAAGG , LRG_507t1:c.-98_-95delinsAAGG	NP_078805.3:n.-98_-95delinsAAGG
XM_006711537.2:c.-98_-95delinsAAGG	XP_006711600.1:n.-98_-95delinsAAGG
XM_006711537.4:c.-98_-95delinsAAGG	XP_006711600.1:n.-98_-95delinsAAGG
XR_001738350.1:n.1551_1554delinsCCTT
NM_024529.5:c.-98_-95delinsAAGG MANE Select	NP_078805.3:n.-98_-95delinsAAGG