Canonical Allele Identifier: CA10580436

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 231210
• ClinVar RCV Id: RCV000216661 ; RCV000444590
• dbSNP Id: rs876659026
• gnomAD v2: 17-33427968-C-T
• gnomAD v3: 17-35100949-C-T
• gnomAD v4: 17-35100949-C-T
• MyVariant Identifiers: chr17:g.33427968C>T (hg19) ; chr17:g.35100949C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35100949C>T , CM000679.2:g.35100949C>T	GRCh38
NC_000017.10:g.33427968C>T , CM000679.1:g.33427968C>T	GRCh37
NC_000017.9:g.30452081C>T	NCBI36
NG_031858.1:g.23921G>A , LRG_516:g.23921G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.*4G>A	ENSP00000468273.3:n.*4G>A
ENST00000587405.6:c.*4G>A	ENSP00000466478.2:n.*4G>A
ENST00000590016.6:c.*4G>A	ENSP00000466399.1:n.*4G>A
ENST00000592577.6:c.*4G>A	ENSP00000466839.2:n.*4G>A
ENST00000345365.11:c.*4G>A MANE Select	ENSP00000338790.6:n.*4G>A
ENST00000335858.11:c.*4G>A	ENSP00000338408.6:n.*4G>A
ENST00000345365.10:c.*4G>A	ENSP00000338790.6:n.*4G>A
ENST00000394589.8:c.*4G>A	ENSP00000378090.4:n.*4G>A
ENST00000460118.6:c.*4G>A	ENSP00000464356.2:n.*4G>A
ENST00000586044.5:c.*722G>A	ENSP00000465584.1:n.*722G>A
ENST00000586210.5:c.*585G>A	ENSP00000465612.1:n.*585G>A
ENST00000587977.5:c.*731G>A	ENSP00000466587.1:n.*731G>A
ENST00000588372.5:c.*474G>A	ENSP00000468764.1:n.*474G>A
ENST00000588594.5:c.*587G>A	ENSP00000465366.1:n.*587G>A
ENST00000590016.5:c.*4G>A	ENSP00000466399.1:n.*4G>A
ENST00000591723.5:c.372+252G>A	ENSP00000467986.1:n.372+252G>A
ENST00000592181.1:c.546+252G>A	ENSP00000464799.1:n.546+252G>A
ENST00000593039.5:c.426+252G>A	ENSP00000466834.1:n.426+252G>A
NM_001142571.1:c.*4G>A	NP_001136043.1:n.*4G>A
NM_002878.3:c.*4G>A , LRG_516t1:c.*4G>A	NP_002869.3:n.*4G>A
NM_133629.2:c.*4G>A	NP_598332.1:n.*4G>A
NR_037711.1:n.1128G>A
NR_037712.1:n.993G>A
NR_037714.1:n.655+252G>A
NM_001142571.2:c.*4G>A	NP_001136043.1:n.*4G>A
NM_133629.3:c.*4G>A	NP_598332.1:n.*4G>A
NR_037711.2:n.1017G>A
NR_037712.2:n.882G>A
NM_002878.4:c.*4G>A MANE Select	NP_002869.3:n.*4G>A