Canonical Allele Identifier: CA1216149978

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203822_193203826delinsACTCC , CM000663.2:g.193203822_193203826delinsACTCC	GRCh38
NC_000001.10:g.193172952_193172956delinsACTCC , CM000663.1:g.193172952_193172956delinsACTCC	GRCh37
NC_000001.9:g.191439575_191439579delinsACTCC	NCBI36
NG_012691.1:g.86865_86869delinsACTCC , LRG_507:g.86865_86869delinsACTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1000_1004delinsACTCC MANE Select	ENSP00000356405.4:p.Thr334=
ENST00000635846.1:c.757_761delinsACTCC	ENSP00000490035.1:p.Thr253=
ENST00000643006.1:c.1068_1072delinsACTCC	ENSP00000496633.1:p.Arg356=
ENST00000648071.1:c.*976_*980delinsACTCC	ENSP00000497513.1:n.*976_*980delinsACTCC
ENST00000649613.1:n.250_254delinsACTCC
ENST00000649895.1:n.1218_1222delinsACTCC
ENST00000650197.1:c.1000_1004delinsACTCC	ENSP00000496929.1:p.Thr334=
ENST00000367435.3:c.1000_1004delinsACTCC	ENSP00000356405.3:p.Thr334=
NM_024529.4:c.1000_1004delinsACTCC , LRG_507t1:c.1000_1004delinsACTCC	NP_078805.3:p.Thr334=
NM_024529.5:c.1000_1004delinsACTCC MANE Select	NP_078805.3:p.Thr334=