LDH info

Canonical Allele Identifier: CA10594462
Gene: BRCA1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 479202
ClinVar RCV Id: RCV000563661

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091776A>G , CM000679.2:g.43091776A>G GRCh38
NC_000017.10:g.41243793A>G , CM000679.1:g.41243793A>G GRCh37
NC_000017.9:g.38497319A>G NCBI36
NG_005905.2:g.126208T>C , LRG_292:g.126208T>C

Transcript Alleles

HGVS Amino-acid change
NM_007294.3:c.3755T>C , LRG_292t1:c.3755T>C NP_009225.1:p.Leu1252Pro
NM_007297.3:c.3614T>C VV NP_009228.2:p.Leu1205Pro
NM_007298.3:c.788-744T>C VV NP_009229.2:p.=
NM_007299.3:c.788-744T>C VV NP_009230.2:p.=
NM_007300.3:c.3755T>C VV NP_009231.2:p.Leu1252Pro
NR_027676.1:n.3891T>C
NM_007294.4:c.3755T>C VV MANE Preferred NP_009225.1:p.Leu1252Pro
NM_007297.4:c.3614T>C VV NP_009228.2:p.Leu1205Pro
NM_007299.4:c.788-744T>C VV NP_009230.2:p.=
NM_007300.4:c.3755T>C VV NP_009231.2:p.Leu1252Pro
NR_027676.2:n.3932T>C
ENST00000352993.7:c.671-744T>C ENSP00000312236.5:p.=
ENST00000354071.7:c.3755T>C ENSP00000326002.7:p.Leu1252Pro
ENST00000357654.7:c.3755T>C ENSP00000350283.3:p.Leu1252Pro
ENST00000461221.5:c.*3538T>C ENSP00000418548.1:p.=
ENST00000461574.1:n.49T>C
ENST00000468300.5:c.788-744T>C ENSP00000417148.1:p.=
ENST00000471181.6:c.3755T>C ENSP00000418960.2:p.Leu1252Pro
ENST00000478531.5:c.785-744T>C ENSP00000420412.1:p.=
ENST00000484087.5:n.410-744T>C ENSP00000419481.1:p.=
ENST00000487825.5:n.413-744T>C ENSP00000418212.1:p.=
ENST00000491747.6:c.788-744T>C ENSP00000420705.2:p.=
ENST00000493795.5:c.3614T>C ENSP00000418775.1:p.Leu1205Pro
ENST00000493919.5:c.647-744T>C ENSP00000418819.1:p.=
ENST00000586385.5:c.5-27825T>C ENSP00000465818.1:p.=
ENST00000591534.5:c.-43-17255T>C ENSP00000467329.1:p.=
ENST00000591849.5:c.-99+33495T>C ENSP00000465347.1:p.=