Canonical Allele Identifier: CA169471

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35119115_35119116insTT , CM000679.2:g.35119115_35119116insTT	GRCh38
NC_000017.10:g.33446134_33446135insTT , CM000679.1:g.33446134_33446135insTT	GRCh37
NC_000017.9:g.30470247_30470248insTT	NCBI36
NG_031858.1:g.5755_5756insAA , LRG_516:g.5755_5756insAA
NG_054719.1:g.2537_2538insTT

Transcript Alleles

HGVS	Amino-acid Change
NM_002878.4:c.140_141insAA MANE Select	NP_002869.3:p.Tyr47Ter
ENST00000345365.11:c.140_141insAA MANE Select	ENSP00000338790.6:p.Tyr47Ter
NM_001142571.1:c.140_141insAA	NP_001136043.1:p.Tyr47Ter
NM_001142571.2:c.140_141insAA	NP_001136043.1:p.Tyr47Ter
NM_002878.3:c.140_141insAA , LRG_516t1:c.140_141insAA	NP_002869.3:p.Tyr47Ter
NM_133629.2:c.140_141insAA	NP_598332.1:p.Tyr47Ter
NM_133629.3:c.140_141insAA	NP_598332.1:p.Tyr47Ter
NR_037711.1:n.396_397insAA
NR_037711.2:n.285_286insAA
NR_037712.1:n.396_397insAA
NR_037712.2:n.285_286insAA
NR_037714.1:n.232+2176_232+2177insAA
ENST00000335858.11:c.140_141insAA	ENSP00000338408.6:p.Tyr47Ter
ENST00000345365.10:c.140_141insAA	ENSP00000338790.6:p.Tyr47Ter
ENST00000394589.8:c.140_141insAA	ENSP00000378090.4:p.Tyr47Ter
ENST00000415064.6:n.290_291insAA
ENST00000460118.6:c.-212_-211insAA	ENSP00000464356.2:n.-212_-211insAA
ENST00000585343.5:c.43_44insAA
ENST00000585947.5:n.159+2176_159+2177insAA
ENST00000585982.5:n.235_236insAA
ENST00000586044.5:c.140_141insAA	ENSP00000465584.1:p.Tyr47Ter
ENST00000586186.2:c.43_44insAA
ENST00000586186.3:c.140_141insAA	ENSP00000468273.3:p.Tyr47Ter
ENST00000586210.5:c.140_141insAA	ENSP00000465612.1:p.Tyr47Ter
ENST00000587405.5:c.-95+2176_-95+2177insAA	ENSP00000466478.1:n.-95+2176_-95+2177insAA
ENST00000587405.6:c.-95+2176_-95+2177insAA	ENSP00000466478.2:n.-95+2176_-95+2177insAA
ENST00000587977.5:c.140_141insAA	ENSP00000466587.1:p.Tyr47Ter
ENST00000587982.5:n.191+2176_191+2177insAA
ENST00000588372.5:c.-95+2176_-95+2177insAA	ENSP00000468764.1:n.-95+2176_-95+2177insAA
ENST00000588594.5:c.140_141insAA	ENSP00000465366.1:p.Tyr47Ter
ENST00000589506.1:n.351_352insAA
ENST00000590016.5:c.140_141insAA	ENSP00000466399.1:p.Tyr47Ter
ENST00000590016.6:c.140_141insAA	ENSP00000466399.1:p.Tyr47Ter
ENST00000590631.1:c.-56_-55insAA	ENSP00000465033.1:n.-56_-55insAA
ENST00000590631.2:n.432_433insAA
ENST00000591723.5:c.-134+2176_-134+2177insAA	ENSP00000467986.1:n.-134+2176_-134+2177insAA
ENST00000592181.1:c.-99_-98insAA	ENSP00000464799.1:n.-99_-98insAA
ENST00000592430.5:n.232+2176_232+2177insAA
ENST00000592577.5:c.146_147insAA	ENSP00000466839.1:p.Tyr49Ter
ENST00000592577.6:c.-218_-217insAA	ENSP00000466839.2:n.-218_-217insAA
ENST00000592850.5:c.43_44insAA
ENST00000592928.2:n.43_44insAA
ENST00000593039.5:c.3+2176_3+2177insAA	ENSP00000466834.1:n.3+2176_3+2177insAA