Canonical Allele Identifier: CA2530403251

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203626_193203627insA , CM000663.2:g.193203626_193203627insA	GRCh38
NC_000001.10:g.193172756_193172757insA , CM000663.1:g.193172756_193172757insA	GRCh37
NC_000001.9:g.191439379_191439380insA	NCBI36
NG_012691.1:g.86669_86670insA , LRG_507:g.86669_86670insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-169_973-168insA MANE Select	ENSP00000356405.4:n.973-169_973-168insA
ENST00000635846.1:c.730-169_730-168insA	ENSP00000490035.1:n.730-169_730-168insA
ENST00000643006.1:c.1041-169_1041-168insA	ENSP00000496633.1:n.1041-169_1041-168insA
ENST00000648071.1:c.*949-169_*949-168insA	ENSP00000497513.1:n.*949-169_*949-168insA
ENST00000649613.1:n.223-169_223-168insA
ENST00000649895.1:n.1191-169_1191-168insA
ENST00000650197.1:c.973-169_973-168insA	ENSP00000496929.1:n.973-169_973-168insA
ENST00000367435.3:c.973-169_973-168insA	ENSP00000356405.3:n.973-169_973-168insA
NM_024529.4:c.973-169_973-168insA , LRG_507t1:c.973-169_973-168insA	NP_078805.3:n.973-169_973-168insA
NM_024529.5:c.973-169_973-168insA MANE Select	NP_078805.3:n.973-169_973-168insA