Canonical Allele Identifier: CA16042158

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 371977
• ClinVar RCV Id: RCV000410381 ; RCV000580898 ; RCV001357020 ; RCV001706622
• dbSNP Id: rs199998187
• gnomAD v2: 17-33428394-A-G
• gnomAD v3: 17-35101375-A-G
• gnomAD v4: 17-35101375-A-G
• MyVariant Identifiers: chr17:g.33428394A>G (hg19) ; chr17:g.35101375A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101375A>G , CM000679.2:g.35101375A>G	GRCh38
NC_000017.10:g.33428394A>G , CM000679.1:g.33428394A>G	GRCh37
NC_000017.9:g.30452507A>G	NCBI36
NG_031858.1:g.23495T>C , LRG_516:g.23495T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.604-10T>C	ENSP00000468273.3:n.604-10T>C
ENST00000587405.6:c.382-10T>C	ENSP00000466478.2:n.382-10T>C
ENST00000590016.6:c.799-10T>C	ENSP00000466399.1:n.799-10T>C
ENST00000592577.6:c.382-10T>C	ENSP00000466839.2:n.382-10T>C
ENST00000345365.11:c.739-10T>C MANE Select	ENSP00000338790.6:n.739-10T>C
ENST00000335858.11:c.403-10T>C	ENSP00000338408.6:n.403-10T>C
ENST00000345365.10:c.739-10T>C	ENSP00000338790.6:n.739-10T>C
ENST00000394589.8:c.739-10T>C	ENSP00000378090.4:n.739-10T>C
ENST00000460118.6:c.208-10T>C	ENSP00000464356.2:n.208-10T>C
ENST00000586044.5:c.*470-10T>C	ENSP00000465584.1:n.*470-10T>C
ENST00000586210.5:c.*333-10T>C	ENSP00000465612.1:n.*333-10T>C
ENST00000587405.5:c.382-10T>C	ENSP00000466478.1:n.382-10T>C
ENST00000587977.5:c.*479-10T>C	ENSP00000466587.1:n.*479-10T>C
ENST00000588372.5:c.*222-10T>C	ENSP00000468764.1:n.*222-10T>C
ENST00000588594.5:c.*335-10T>C	ENSP00000465366.1:n.*335-10T>C
ENST00000590016.5:c.799-10T>C	ENSP00000466399.1:n.799-10T>C
ENST00000591723.5:c.208-10T>C	ENSP00000467986.1:n.208-10T>C
ENST00000592181.1:c.382-10T>C	ENSP00000464799.1:n.382-10T>C
ENST00000592577.5:c.745-10T>C	ENSP00000466839.1:n.745-10T>C
ENST00000593039.5:c.262-10T>C	ENSP00000466834.1:n.262-10T>C
NM_001142571.1:c.799-10T>C	NP_001136043.1:n.799-10T>C
NM_002878.3:c.739-10T>C , LRG_516t1:c.739-10T>C	NP_002869.3:n.739-10T>C
NM_133629.2:c.403-10T>C	NP_598332.1:n.403-10T>C
NR_037711.1:n.876-10T>C
NR_037712.1:n.741-10T>C
NR_037714.1:n.491-10T>C
NM_001142571.2:c.799-10T>C	NP_001136043.1:n.799-10T>C
NM_133629.3:c.403-10T>C	NP_598332.1:n.403-10T>C
NR_037711.2:n.765-10T>C
NR_037712.2:n.630-10T>C
NM_002878.4:c.739-10T>C MANE Select	NP_002869.3:n.739-10T>C