Canonical Allele Identifier: CA2649624598

Gene: CDC73

Linked Data

• gnomAD v4: 1-193122064-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122064G>T , CM000663.2:g.193122064G>T	GRCh38
NC_000001.10:g.193091194G>T , CM000663.1:g.193091194G>T	GRCh37
NC_000001.9:g.191357817G>T	NCBI36
NG_012691.1:g.5107G>T , LRG_507:g.5107G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-137G>T MANE Select	ENSP00000356405.4:n.-137G>T
ENST00000643006.1:c.-137G>T	ENSP00000496633.1:n.-137G>T
ENST00000649895.1:n.82G>T
ENST00000367435.3:c.-137G>T	ENSP00000356405.3:n.-137G>T
NM_024529.4:c.-137G>T , LRG_507t1:c.-137G>T	NP_078805.3:n.-137G>T
XM_006711537.2:c.-137G>T	XP_006711600.1:n.-137G>T
XM_006711537.4:c.-137G>T	XP_006711600.1:n.-137G>T
XR_001738350.1:n.1593C>A
NM_024529.5:c.-137G>T MANE Select	NP_078805.3:n.-137G>T