LDH info

Canonical Allele Identifier: CA219128

Identifiers and link-outs to other resources

ClinVar Variation Id: 68187
dbSNP Id: rs281875250

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288460C>T , CM000666.2:g.186288460C>T GRCh38
NC_000004.11:g.187209614C>T , CM000666.1:g.187209614C>T GRCh37
NC_000004.10:g.187446608C>T NCBI36
NG_008051.1:g.27497C>T , LRG_583:g.27497C>T

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.1724C>T , LRG_583t1:c.1724C>T (F11) NP_000119.1:p.Ser575Leu
NR_033900.1:n.1034G>A (F11-AS1)
XM_005262821.2:c.1727C>T (F11) XP_005262878.1:p.Ser576Leu
XM_005262822.2:c.1631C>T (F11) XP_005262879.1:p.Ser544Leu
XM_005262823.2:c.1457C>T (F11) XP_005262880.1:p.Ser486Leu
XM_006714137.1:c.1679C>T (F11) XP_006714200.1:p.Ser560Leu
XM_005262821.4:c.1727C>T (F11) XP_005262878.1:p.Ser576Leu
XM_005262822.4:c.1631C>T (F11) XP_005262879.1:p.Ser544Leu
XM_005262823.4:c.1457C>T (F11) XP_005262880.1:p.Ser486Leu
XM_006714137.3:c.1679C>T (F11) XP_006714200.1:p.Ser560Leu
NM_000128.4:c.1724C>T (F11) VV NP_000119.1:p.Ser575Leu
ENST00000264691.4:n.324C>T
ENST00000264692.8:c.1562C>T ENSP00000264692.5:p.Ser521Leu
ENST00000403665.6:c.1724C>T ENSP00000384957.2:p.Ser575Leu
ENST00000503841.1:n.243C>T