Canonical Allele Identifier: CA399089411

Gene: RAD51D

Linked Data

• MyVariant Identifiers: chr17:g.33434142C>A (hg19) ; chr17:g.35107123C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107123C>A , CM000679.2:g.35107123C>A	GRCh38
NC_000017.10:g.33434142C>A , CM000679.1:g.33434142C>A	GRCh37
NC_000017.9:g.30458255C>A	NCBI36
NG_031858.1:g.17747G>T , LRG_516:g.17747G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+243G>T	ENSP00000468273.3:n.345+243G>T
ENST00000587405.6:c.-12-1G>T	ENSP00000466478.2:n.-12-1G>T
ENST00000590016.6:c.406-1G>T	ENSP00000466399.1:n.406-1G>T
ENST00000590631.2:n.437-642G>T
ENST00000592577.6:c.-12-1G>T	ENSP00000466839.2:n.-12-1G>T
ENST00000345365.11:c.346-1G>T MANE Select	ENSP00000338790.6:n.346-1G>T
ENST00000335858.11:c.145-642G>T	ENSP00000338408.6:n.145-642G>T
ENST00000345365.10:c.346-1G>T	ENSP00000338790.6:n.346-1G>T
ENST00000394589.8:c.346-1G>T	ENSP00000378090.4:n.346-1G>T
ENST00000415064.6:n.496-1G>T
ENST00000460118.6:c.-125-62G>T	ENSP00000464356.2:n.-125-62G>T
ENST00000585343.5:c.428-1G>T
ENST00000585947.5:n.242-1G>T
ENST00000585982.5:n.500+243G>T
ENST00000586044.5:c.*77-1G>T	ENSP00000465584.1:n.*77-1G>T
ENST00000586186.2:c.248+243G>T
ENST00000586210.5:c.264-1G>T	ENSP00000465612.1:n.264-1G>T
ENST00000587405.5:c.-12-1G>T	ENSP00000466478.1:n.-12-1G>T
ENST00000587977.5:c.*86-1G>T	ENSP00000466587.1:n.*86-1G>T
ENST00000587982.5:n.273+243G>T
ENST00000588372.5:c.-12-1G>T	ENSP00000468764.1:n.-12-1G>T
ENST00000588594.5:c.*76+243G>T	ENSP00000465366.1:n.*76+243G>T
ENST00000590016.5:c.406-1G>T	ENSP00000466399.1:n.406-1G>T
ENST00000590631.1:c.-51-642G>T	ENSP00000465033.1:n.-51-642G>T
ENST00000591723.5:c.-52+243G>T	ENSP00000467986.1:n.-52+243G>T
ENST00000592181.1:c.-12-1G>T	ENSP00000464799.1:n.-12-1G>T
ENST00000592430.5:n.315-1G>T
ENST00000592577.5:c.352-1G>T	ENSP00000466839.1:n.352-1G>T
ENST00000592850.5:c.346-642G>T
ENST00000592928.2:n.167-642G>T
ENST00000593039.5:c.4-642G>T	ENSP00000466834.1:n.4-642G>T
NM_001142571.1:c.406-1G>T	NP_001136043.1:n.406-1G>T
NM_002878.3:c.346-1G>T , LRG_516t1:c.346-1G>T	NP_002869.3:n.346-1G>T
NM_133629.2:c.145-642G>T	NP_598332.1:n.145-642G>T
NR_037711.1:n.483-1G>T
NR_037712.1:n.482+243G>T
NR_037714.1:n.233-642G>T
NM_001142571.2:c.406-1G>T	NP_001136043.1:n.406-1G>T
NM_133629.3:c.145-642G>T	NP_598332.1:n.145-642G>T
NR_037711.2:n.372-1G>T
NR_037712.2:n.371+243G>T
NM_002878.4:c.346-1G>T MANE Select	NP_002869.3:n.346-1G>T