LDH info

Canonical Allele Identifier: CA10599839
Gene: BRCA1 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094422A>T , CM000679.2:g.43094422A>T GRCh38
NC_000017.10:g.41246439A>T , CM000679.1:g.41246439A>T GRCh37
NC_000017.9:g.38499965A>T NCBI36
NG_005905.2:g.123562T>A , LRG_292:g.123562T>A

Transcript Alleles

HGVS Amino-acid change
NM_007294.3:c.1109T>A , LRG_292t1:c.1109T>A NP_009225.1:p.Val370Asp
NM_007297.3:c.968T>A VV NP_009228.2:p.Val323Asp
NM_007298.3:c.787+322T>A VV NP_009229.2:p.=
NM_007299.3:c.787+322T>A VV NP_009230.2:p.=
NM_007300.3:c.1109T>A VV NP_009231.2:p.Val370Asp
NR_027676.1:n.1245T>A
NM_007294.4:c.1109T>A VV MANE Preferred NP_009225.1:p.Val370Asp
NM_007297.4:c.968T>A VV NP_009228.2:p.Val323Asp
NM_007299.4:c.787+322T>A VV NP_009230.2:p.=
NM_007300.4:c.1109T>A VV NP_009231.2:p.Val370Asp
NR_027676.2:n.1286T>A
ENST00000352993.7:c.670+1424T>A ENSP00000312236.5:p.=
ENST00000354071.7:c.1109T>A ENSP00000326002.7:p.Val370Asp
ENST00000357654.7:c.1109T>A ENSP00000350283.3:p.Val370Asp
ENST00000412061.3:n.460T>A
ENST00000461221.5:c.*892T>A ENSP00000418548.1:p.=
ENST00000468300.5:c.787+322T>A ENSP00000417148.1:p.=
ENST00000470026.5:c.1109T>A ENSP00000419274.1:p.Val370Asp
ENST00000471181.6:c.1109T>A ENSP00000418960.2:p.Val370Asp
ENST00000473961.5:n.706T>A
ENST00000477152.5:c.1031T>A ENSP00000419988.1:p.Val344Asp
ENST00000478531.5:c.784+322T>A ENSP00000420412.1:p.=
ENST00000484087.5:n.409+322T>A ENSP00000419481.1:p.=
ENST00000487825.5:n.412+322T>A ENSP00000418212.1:p.=
ENST00000491747.6:c.787+322T>A ENSP00000420705.2:p.=
ENST00000492859.5:c.*1045T>A ENSP00000420253.1:p.=
ENST00000493795.5:c.968T>A ENSP00000418775.1:p.Val323Asp
ENST00000493919.5:c.646+322T>A ENSP00000418819.1:p.=
ENST00000494123.5:c.1109T>A ENSP00000419103.1:p.Val370Asp
ENST00000497488.1:c.221T>A ENSP00000418986.1:p.Val74Asp
ENST00000586385.5:c.5-30471T>A ENSP00000465818.1:p.=
ENST00000591534.5:c.-43-19901T>A ENSP00000467329.1:p.=
ENST00000591849.5:c.-99+30849T>A ENSP00000465347.1:p.=
ENST00000634433.1:c.986T>A ENSP00000489431.1:p.Val329Asp