Canonical Allele Identifier: CA2733456786
Gene: RAD51D HGNC NCBI

Linked Data

dbSNP Id: rs2142434325

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35107143T>A , CM000679.2:g.35107143T>A GRCh38
NC_000017.10:g.33434162T>A , CM000679.1:g.33434162T>A GRCh37
NC_000017.9:g.30458275T>A NCBI36
NG_031858.1:g.17727A>T , LRG_516:g.17727A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.345+223A>T ENSP00000468273.3:n.345+223A>T
ENST00000587405.6:c.-12-21A>T ENSP00000466478.2:n.-12-21A>T
ENST00000590016.6:c.406-21A>T ENSP00000466399.1:n.406-21A>T
ENST00000590631.2:n.437-662A>T
ENST00000592577.6:c.-12-21A>T ENSP00000466839.2:n.-12-21A>T
ENST00000345365.11:c.346-21A>T MANE Select ENSP00000338790.6:n.346-21A>T
ENST00000335858.11:c.145-662A>T ENSP00000338408.6:n.145-662A>T
ENST00000345365.10:c.346-21A>T ENSP00000338790.6:n.346-21A>T
ENST00000394589.8:c.346-21A>T ENSP00000378090.4:n.346-21A>T
ENST00000415064.6:n.496-21A>T
ENST00000460118.6:c.-125-82A>T ENSP00000464356.2:n.-125-82A>T
ENST00000585343.5:c.428-21A>T
ENST00000585947.5:n.242-21A>T
ENST00000585982.5:n.500+223A>T
ENST00000586044.5:c.*77-21A>T ENSP00000465584.1:n.*77-21A>T
ENST00000586186.2:c.248+223A>T
ENST00000586210.5:c.264-21A>T ENSP00000465612.1:n.264-21A>T
ENST00000587405.5:c.-12-21A>T ENSP00000466478.1:n.-12-21A>T
ENST00000587977.5:c.*86-21A>T ENSP00000466587.1:n.*86-21A>T
ENST00000587982.5:n.273+223A>T
ENST00000588372.5:c.-12-21A>T ENSP00000468764.1:n.-12-21A>T
ENST00000588594.5:c.*76+223A>T ENSP00000465366.1:n.*76+223A>T
ENST00000590016.5:c.406-21A>T ENSP00000466399.1:n.406-21A>T
ENST00000590631.1:c.-51-662A>T ENSP00000465033.1:n.-51-662A>T
ENST00000591723.5:c.-52+223A>T ENSP00000467986.1:n.-52+223A>T
ENST00000592181.1:c.-12-21A>T ENSP00000464799.1:n.-12-21A>T
ENST00000592430.5:n.315-21A>T
ENST00000592577.5:c.352-21A>T ENSP00000466839.1:n.352-21A>T
ENST00000592850.5:c.346-662A>T
ENST00000592928.2:n.167-662A>T
ENST00000593039.5:c.4-662A>T ENSP00000466834.1:n.4-662A>T
NM_001142571.1:c.406-21A>T NP_001136043.1:n.406-21A>T
NM_002878.3:c.346-21A>T , LRG_516t1:c.346-21A>T NP_002869.3:n.346-21A>T
NM_133629.2:c.145-662A>T NP_598332.1:n.145-662A>T
NR_037711.1:n.483-21A>T
NR_037712.1:n.482+223A>T
NR_037714.1:n.233-662A>T
NM_001142571.2:c.406-21A>T NP_001136043.1:n.406-21A>T
NM_133629.3:c.145-662A>T NP_598332.1:n.145-662A>T
NR_037711.2:n.372-21A>T
NR_037712.2:n.371+223A>T
NM_002878.4:c.346-21A>T MANE Select NP_002869.3:n.346-21A>T