Canonical Allele Identifier: CA2573153504

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 1550481
• ClinVar RCV Id: RCV002189727
• dbSNP Id: rs2142431838

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106969C>T , CM000679.2:g.35106969C>T	GRCh38
NC_000017.10:g.33433988C>T , CM000679.1:g.33433988C>T	GRCh37
NC_000017.9:g.30458101C>T	NCBI36
NG_031858.1:g.17901G>A , LRG_516:g.17901G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+397G>A	ENSP00000468273.3:n.345+397G>A
ENST00000587405.6:c.123+19G>A	ENSP00000466478.2:n.123+19G>A
ENST00000590016.6:c.540+19G>A	ENSP00000466399.1:n.540+19G>A
ENST00000590631.2:n.437-488G>A
ENST00000592577.6:c.123+19G>A	ENSP00000466839.2:n.123+19G>A
ENST00000345365.11:c.480+19G>A MANE Select	ENSP00000338790.6:n.480+19G>A
ENST00000335858.11:c.145-488G>A	ENSP00000338408.6:n.145-488G>A
ENST00000345365.10:c.480+19G>A	ENSP00000338790.6:n.480+19G>A
ENST00000394589.8:c.480+19G>A	ENSP00000378090.4:n.480+19G>A
ENST00000415064.6:n.630+19G>A
ENST00000460118.6:c.-52+19G>A	ENSP00000464356.2:n.-52+19G>A
ENST00000585343.5:c.562+19G>A
ENST00000585947.5:n.376+19G>A
ENST00000585982.5:n.500+397G>A
ENST00000586044.5:c.*211+19G>A	ENSP00000465584.1:n.*211+19G>A
ENST00000586186.2:c.248+397G>A
ENST00000586210.5:c.*74+19G>A	ENSP00000465612.1:n.*74+19G>A
ENST00000587405.5:c.123+19G>A	ENSP00000466478.1:n.123+19G>A
ENST00000587977.5:c.*220+19G>A	ENSP00000466587.1:n.*220+19G>A
ENST00000587982.5:n.273+397G>A
ENST00000588372.5:c.123+19G>A	ENSP00000468764.1:n.123+19G>A
ENST00000588594.5:c.*76+397G>A	ENSP00000465366.1:n.*76+397G>A
ENST00000590016.5:c.540+19G>A	ENSP00000466399.1:n.540+19G>A
ENST00000590631.1:c.-51-488G>A	ENSP00000465033.1:n.-51-488G>A
ENST00000591723.5:c.-52+397G>A	ENSP00000467986.1:n.-52+397G>A
ENST00000592181.1:c.123+19G>A	ENSP00000464799.1:n.123+19G>A
ENST00000592430.5:n.449+19G>A
ENST00000592577.5:c.486+19G>A	ENSP00000466839.1:n.486+19G>A
ENST00000592850.5:c.346-488G>A
ENST00000592928.2:n.167-488G>A
ENST00000593039.5:c.4-488G>A	ENSP00000466834.1:n.4-488G>A
NM_001142571.1:c.540+19G>A	NP_001136043.1:n.540+19G>A
NM_002878.3:c.480+19G>A , LRG_516t1:c.480+19G>A	NP_002869.3:n.480+19G>A
NM_133629.2:c.145-488G>A	NP_598332.1:n.145-488G>A
NR_037711.1:n.617+19G>A
NR_037712.1:n.482+397G>A
NR_037714.1:n.233-488G>A
NM_001142571.2:c.540+19G>A	NP_001136043.1:n.540+19G>A
NM_133629.3:c.145-488G>A	NP_598332.1:n.145-488G>A
NR_037711.2:n.506+19G>A
NR_037712.2:n.371+397G>A
NM_002878.4:c.480+19G>A MANE Select	NP_002869.3:n.480+19G>A