Canonical Allele Identifier: CA1303222

Gene: CDC73

Linked Data

• dbSNP Id: rs753057198
• ExAC: 1:193091310 G / A
• gnomAD v2: 1-193091310-G-A
• gnomAD v4: 1-193122180-G-A
• MyVariant Identifiers: chr1:g.193091310G>A (hg19) ; chr1:g.193122180G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122180G>A , CM000663.2:g.193122180G>A	GRCh38
NC_000001.10:g.193091310G>A , CM000663.1:g.193091310G>A	GRCh37
NC_000001.9:g.191357933G>A	NCBI36
NG_012691.1:g.5223G>A , LRG_507:g.5223G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-21G>A MANE Select	ENSP00000356405.4:n.-21G>A
ENST00000635846.1:c.-21G>A	ENSP00000490035.1:n.-21G>A
ENST00000643006.1:c.-21G>A	ENSP00000496633.1:n.-21G>A
ENST00000643784.1:c.-21G>A	ENSP00000494944.1:n.-21G>A
ENST00000648071.1:c.-21G>A	ENSP00000497513.1:n.-21G>A
ENST00000649895.1:n.198G>A
ENST00000650197.1:c.-21G>A	ENSP00000496929.1:n.-21G>A
ENST00000367435.3:c.-21G>A	ENSP00000356405.3:n.-21G>A
NM_024529.4:c.-21G>A , LRG_507t1:c.-21G>A	NP_078805.3:n.-21G>A
XM_006711537.2:c.-21G>A	XP_006711600.1:n.-21G>A
XM_006711537.4:c.-21G>A	XP_006711600.1:n.-21G>A
XR_001738350.1:n.1477C>T
NM_024529.5:c.-21G>A MANE Select	NP_078805.3:n.-21G>A