Canonical Allele Identifier: CA625549082

Gene: RAD51D

Linked Data

• dbSNP Id: rs1426666641
• gnomAD v2: 17-33433918-G-A
• gnomAD v3: 17-35106899-G-A
• gnomAD v4: 17-35106899-G-A
• MyVariant Identifiers: chr17:g.33433918G>A (hg19) ; chr17:g.35106899G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106899G>A , CM000679.2:g.35106899G>A	GRCh38
NC_000017.10:g.33433918G>A , CM000679.1:g.33433918G>A	GRCh37
NC_000017.9:g.30458031G>A	NCBI36
NG_031858.1:g.17971C>T , LRG_516:g.17971C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.346-418C>T	ENSP00000468273.3:n.346-418C>T
ENST00000587405.6:c.123+89C>T	ENSP00000466478.2:n.123+89C>T
ENST00000590016.6:c.540+89C>T	ENSP00000466399.1:n.540+89C>T
ENST00000590631.2:n.437-418C>T
ENST00000592577.6:c.123+89C>T	ENSP00000466839.2:n.123+89C>T
ENST00000345365.11:c.480+89C>T MANE Select	ENSP00000338790.6:n.480+89C>T
ENST00000335858.11:c.145-418C>T	ENSP00000338408.6:n.145-418C>T
ENST00000345365.10:c.480+89C>T	ENSP00000338790.6:n.480+89C>T
ENST00000394589.8:c.480+89C>T	ENSP00000378090.4:n.480+89C>T
ENST00000415064.6:n.630+89C>T
ENST00000460118.6:c.-52+89C>T	ENSP00000464356.2:n.-52+89C>T
ENST00000585343.5:c.562+89C>T
ENST00000585947.5:n.376+89C>T
ENST00000585982.5:n.501-418C>T
ENST00000586044.5:c.*211+89C>T	ENSP00000465584.1:n.*211+89C>T
ENST00000586186.2:c.249-418C>T
ENST00000586210.5:c.*74+89C>T	ENSP00000465612.1:n.*74+89C>T
ENST00000587405.5:c.123+89C>T	ENSP00000466478.1:n.123+89C>T
ENST00000587977.5:c.*220+89C>T	ENSP00000466587.1:n.*220+89C>T
ENST00000587982.5:n.274-418C>T
ENST00000588372.5:c.123+89C>T	ENSP00000468764.1:n.123+89C>T
ENST00000588594.5:c.*77-418C>T	ENSP00000465366.1:n.*77-418C>T
ENST00000590016.5:c.540+89C>T	ENSP00000466399.1:n.540+89C>T
ENST00000590631.1:c.-51-418C>T	ENSP00000465033.1:n.-51-418C>T
ENST00000591723.5:c.-51-418C>T	ENSP00000467986.1:n.-51-418C>T
ENST00000592181.1:c.123+89C>T	ENSP00000464799.1:n.123+89C>T
ENST00000592430.5:n.449+89C>T
ENST00000592577.5:c.486+89C>T	ENSP00000466839.1:n.486+89C>T
ENST00000592850.5:c.346-418C>T
ENST00000592928.2:n.167-418C>T
ENST00000593039.5:c.4-418C>T	ENSP00000466834.1:n.4-418C>T
NM_001142571.1:c.540+89C>T	NP_001136043.1:n.540+89C>T
NM_002878.3:c.480+89C>T , LRG_516t1:c.480+89C>T	NP_002869.3:n.480+89C>T
NM_133629.2:c.145-418C>T	NP_598332.1:n.145-418C>T
NR_037711.1:n.617+89C>T
NR_037712.1:n.483-418C>T
NR_037714.1:n.233-418C>T
NM_001142571.2:c.540+89C>T	NP_001136043.1:n.540+89C>T
NM_133629.3:c.145-418C>T	NP_598332.1:n.145-418C>T
NR_037711.2:n.506+89C>T
NR_037712.2:n.372-418C>T
NM_002878.4:c.480+89C>T MANE Select	NP_002869.3:n.480+89C>T