Canonical Allele Identifier: CA499731756

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 1159891
• ClinVar RCV Id: RCV001503811 ; RCV002334554
• dbSNP Id: rs2142433941
• gnomAD v4: 17-35107114-G-A
• COSMIC: COSM4493426 ; COSM4493427
• MyVariant Identifiers: chr17:g.33434133G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107114G>A , CM000679.2:g.35107114G>A	GRCh38
NC_000017.10:g.33434133G>A , CM000679.1:g.33434133G>A	GRCh37
NC_000017.9:g.30458246G>A	NCBI36
NG_031858.1:g.17756C>T , LRG_516:g.17756C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+252C>T	ENSP00000468273.3:n.345+252C>T
ENST00000587405.6:c.-4C>T	ENSP00000466478.2:n.-4C>T
ENST00000590016.6:c.414C>T	ENSP00000466399.1:p.Leu138=
ENST00000590631.2:n.437-633C>T
ENST00000592577.6:c.-4C>T	ENSP00000466839.2:n.-4C>T
ENST00000345365.11:c.354C>T MANE Select	ENSP00000338790.6:p.Leu118=
ENST00000335858.11:c.145-633C>T	ENSP00000338408.6:n.145-633C>T
ENST00000345365.10:c.354C>T	ENSP00000338790.6:p.Leu118=
ENST00000394589.8:c.354C>T	ENSP00000378090.4:p.Leu118=
ENST00000415064.6:n.504C>T
ENST00000460118.6:c.-125-53C>T	ENSP00000464356.2:n.-125-53C>T
ENST00000585343.5:c.436C>T
ENST00000585947.5:n.250C>T
ENST00000585982.5:n.500+252C>T
ENST00000586044.5:c.*85C>T	ENSP00000465584.1:n.*85C>T
ENST00000586186.2:c.248+252C>T
ENST00000586210.5:c.272C>T	ENSP00000465612.1:p.Ser91Phe
ENST00000587405.5:c.-4C>T	ENSP00000466478.1:n.-4C>T
ENST00000587977.5:c.*94C>T	ENSP00000466587.1:n.*94C>T
ENST00000587982.5:n.273+252C>T
ENST00000588372.5:c.-4C>T	ENSP00000468764.1:n.-4C>T
ENST00000588594.5:c.*76+252C>T	ENSP00000465366.1:n.*76+252C>T
ENST00000590016.5:c.414C>T	ENSP00000466399.1:p.Leu138=
ENST00000590631.1:c.-51-633C>T	ENSP00000465033.1:n.-51-633C>T
ENST00000591723.5:c.-52+252C>T	ENSP00000467986.1:n.-52+252C>T
ENST00000592181.1:c.-4C>T	ENSP00000464799.1:n.-4C>T
ENST00000592430.5:n.323C>T
ENST00000592577.5:c.360C>T	ENSP00000466839.1:p.Leu120=
ENST00000592850.5:c.346-633C>T
ENST00000592928.2:n.167-633C>T
ENST00000593039.5:c.4-633C>T	ENSP00000466834.1:n.4-633C>T
NM_001142571.1:c.414C>T	NP_001136043.1:p.Leu138=
NM_002878.3:c.354C>T , LRG_516t1:c.354C>T	NP_002869.3:p.Leu118=
NM_133629.2:c.145-633C>T	NP_598332.1:n.145-633C>T
NR_037711.1:n.491C>T
NR_037712.1:n.482+252C>T
NR_037714.1:n.233-633C>T
NM_001142571.2:c.414C>T	NP_001136043.1:p.Leu138=
NM_133629.3:c.145-633C>T	NP_598332.1:n.145-633C>T
NR_037711.2:n.380C>T
NR_037712.2:n.371+252C>T
NM_002878.4:c.354C>T MANE Select	NP_002869.3:p.Leu118=