LDH info

Canonical Allele Identifier: CA279976
Gene: BRAF HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13979
dbSNP Id: rs180177040

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140754187T>C , CM000669.2:g.140754187T>C GRCh38
NC_000007.13:g.140453987T>C , CM000669.1:g.140453987T>C GRCh37
NC_000007.12:g.140100456T>C NCBI36
NG_007873.3:g.175578A>G , LRG_299:g.175578A>G

Transcript Alleles

HGVS Amino-acid change
NM_004333.4:c.1741A>G , LRG_299t1:c.1741A>G NP_004324.2:p.Asn581Asp
XM_005250045.1:c.1741A>G XP_005250102.1:p.Asn581Asp
XM_005250046.1:c.1741A>G XP_005250103.1:p.Asn581Asp
XM_011516529.1:c.1741A>G XP_011514831.1:p.Asn581Asp
XM_011516530.1:c.1695-4769A>G XP_011514832.1:p.=
XR_242190.1:n.1749A>G
XR_927520.1:n.1749A>G
XR_927521.1:n.1749A>G
XR_927522.1:n.1703-4769A>G
XR_927523.1:n.1703-4769A>G
NM_001354609.1:c.1741A>G VV NP_001341538.1:p.Asn581Asp
NM_004333.5:c.1741A>G VV NP_004324.2:p.Asn581Asp
NR_148928.1:n.2046A>G
XM_017012558.1:c.1861A>G XP_016868047.1:p.Asn621Asp
XM_017012559.1:c.1861A>G XP_016868048.1:p.Asn621Asp
XR_001744857.1:n.1869A>G
XR_001744858.1:n.1823-4769A>G
NM_001354609.2:c.1741A>G VV NP_001341538.1:p.Asn581Asp
NM_001374244.1:c.1861A>G VV NP_001361173.1:p.Asn621Asp
NM_001374258.1:c.1861A>G VV NP_001361187.1:p.Asn621Asp
NM_004333.6:c.1741A>G VV NP_004324.2:p.Asn581Asp
ENST00000288602.10:c.1741A>G ENSP00000288602.6:p.Asn581Asp
ENST00000479537.5:n.25A>G ENSP00000418033.1:p.Asn9Asp
ENST00000496384.6:n.564A>G
ENST00000497784.1:n.1776A>G ENSP00000420119.1:p.=