Canonical Allele Identifier: CA729344043

Gene: CDC73

Linked Data

• dbSNP Id: rs1424881795
• gnomAD v3: 1-193122146-G-T
• gnomAD v4: 1-193122146-G-T
• MyVariant Identifiers: chr1:g.193091276G>T (hg19) ; chr1:g.193122146G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122146G>T , CM000663.2:g.193122146G>T	GRCh38
NC_000001.10:g.193091276G>T , CM000663.1:g.193091276G>T	GRCh37
NC_000001.9:g.191357899G>T	NCBI36
NG_012691.1:g.5189G>T , LRG_507:g.5189G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-55G>T MANE Select	ENSP00000356405.4:n.-55G>T
ENST00000643006.1:c.-55G>T	ENSP00000496633.1:n.-55G>T
ENST00000643784.1:c.-55G>T	ENSP00000494944.1:n.-55G>T
ENST00000649895.1:n.164G>T
ENST00000650197.1:c.-55G>T	ENSP00000496929.1:n.-55G>T
ENST00000367435.3:c.-55G>T	ENSP00000356405.3:n.-55G>T
NM_024529.4:c.-55G>T , LRG_507t1:c.-55G>T	NP_078805.3:n.-55G>T
XM_006711537.2:c.-55G>T	XP_006711600.1:n.-55G>T
XM_006711537.4:c.-55G>T	XP_006711600.1:n.-55G>T
XR_001738350.1:n.1511C>A
NM_024529.5:c.-55G>T MANE Select	NP_078805.3:n.-55G>T