LDH info

Canonical Allele Identifier: CA001915
Gene: BRCA1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 37493
dbSNP Id: rs80357115

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092597A>C , CM000679.2:g.43092597A>C GRCh38
NC_000017.10:g.41244614A>C , CM000679.1:g.41244614A>C GRCh37
NC_000017.9:g.38498140A>C NCBI36
NG_005905.2:g.125387T>G , LRG_292:g.125387T>G

Transcript Alleles

HGVS Amino-acid change
NM_007294.3:c.2934T>G , LRG_292t1:c.2934T>G NP_009225.1:p.Tyr978Ter
NM_007297.3:c.2793T>G VV NP_009228.2:p.Tyr931Ter
NM_007298.3:c.788-1565T>G VV NP_009229.2:p.=
NM_007299.3:c.788-1565T>G VV NP_009230.2:p.=
NM_007300.3:c.2934T>G VV NP_009231.2:p.Tyr978Ter
NR_027676.1:n.3070T>G
ENST00000352993.7:c.671-1565T>G ENSP00000312236.5:p.=
ENST00000354071.7:c.2934T>G ENSP00000326002.7:p.Tyr978Ter
ENST00000357654.7:c.2934T>G ENSP00000350283.3:p.Tyr978Ter
ENST00000461221.5:c.*2717T>G ENSP00000418548.1:p.=
ENST00000468300.5:c.788-1565T>G ENSP00000417148.1:p.=
ENST00000471181.6:c.2934T>G ENSP00000418960.2:p.Tyr978Ter
ENST00000478531.5:c.785-1565T>G ENSP00000420412.1:p.=
ENST00000484087.5:n.410-1565T>G ENSP00000419481.1:p.=
ENST00000487825.5:n.413-1565T>G ENSP00000418212.1:p.=
ENST00000491747.6:c.788-1565T>G ENSP00000420705.2:p.=
ENST00000493795.5:c.2793T>G ENSP00000418775.1:p.Tyr931Ter
ENST00000493919.5:c.647-1565T>G ENSP00000418819.1:p.=
ENST00000586385.5:c.5-28646T>G ENSP00000465818.1:p.=
ENST00000591534.5:c.-43-18076T>G ENSP00000467329.1:p.=
ENST00000591849.5:c.-99+32674T>G ENSP00000465347.1:p.=