Canonical Allele Identifier: CA2637246453

Gene: RAD51D

Linked Data

• gnomAD v4: 17-35106893-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106893A>G , CM000679.2:g.35106893A>G	GRCh38
NC_000017.10:g.33433912A>G , CM000679.1:g.33433912A>G	GRCh37
NC_000017.9:g.30458025A>G	NCBI36
NG_031858.1:g.17977T>C , LRG_516:g.17977T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.346-412T>C	ENSP00000468273.3:n.346-412T>C
ENST00000587405.6:c.123+95T>C	ENSP00000466478.2:n.123+95T>C
ENST00000590016.6:c.540+95T>C	ENSP00000466399.1:n.540+95T>C
ENST00000590631.2:n.437-412T>C
ENST00000592577.6:c.123+95T>C	ENSP00000466839.2:n.123+95T>C
ENST00000345365.11:c.480+95T>C MANE Select	ENSP00000338790.6:n.480+95T>C
ENST00000335858.11:c.145-412T>C	ENSP00000338408.6:n.145-412T>C
ENST00000345365.10:c.480+95T>C	ENSP00000338790.6:n.480+95T>C
ENST00000394589.8:c.480+95T>C	ENSP00000378090.4:n.480+95T>C
ENST00000415064.6:n.630+95T>C
ENST00000460118.6:c.-52+95T>C	ENSP00000464356.2:n.-52+95T>C
ENST00000585343.5:c.562+95T>C
ENST00000585947.5:n.376+95T>C
ENST00000585982.5:n.501-412T>C
ENST00000586044.5:c.*211+95T>C	ENSP00000465584.1:n.*211+95T>C
ENST00000586186.2:c.249-412T>C
ENST00000586210.5:c.*74+95T>C	ENSP00000465612.1:n.*74+95T>C
ENST00000587405.5:c.123+95T>C	ENSP00000466478.1:n.123+95T>C
ENST00000587977.5:c.*220+95T>C	ENSP00000466587.1:n.*220+95T>C
ENST00000587982.5:n.274-412T>C
ENST00000588372.5:c.123+95T>C	ENSP00000468764.1:n.123+95T>C
ENST00000588594.5:c.*77-412T>C	ENSP00000465366.1:n.*77-412T>C
ENST00000590016.5:c.540+95T>C	ENSP00000466399.1:n.540+95T>C
ENST00000590631.1:c.-51-412T>C	ENSP00000465033.1:n.-51-412T>C
ENST00000591723.5:c.-51-412T>C	ENSP00000467986.1:n.-51-412T>C
ENST00000592181.1:c.123+95T>C	ENSP00000464799.1:n.123+95T>C
ENST00000592430.5:n.449+95T>C
ENST00000592577.5:c.486+95T>C	ENSP00000466839.1:n.486+95T>C
ENST00000592850.5:c.346-412T>C
ENST00000592928.2:n.167-412T>C
ENST00000593039.5:c.4-412T>C	ENSP00000466834.1:n.4-412T>C
NM_001142571.1:c.540+95T>C	NP_001136043.1:n.540+95T>C
NM_002878.3:c.480+95T>C , LRG_516t1:c.480+95T>C	NP_002869.3:n.480+95T>C
NM_133629.2:c.145-412T>C	NP_598332.1:n.145-412T>C
NR_037711.1:n.617+95T>C
NR_037712.1:n.483-412T>C
NR_037714.1:n.233-412T>C
NM_001142571.2:c.540+95T>C	NP_001136043.1:n.540+95T>C
NM_133629.3:c.145-412T>C	NP_598332.1:n.145-412T>C
NR_037711.2:n.506+95T>C
NR_037712.2:n.372-412T>C
NM_002878.4:c.480+95T>C MANE Select	NP_002869.3:n.480+95T>C