LDH info

Canonical Allele Identifier: CA121765
Gene: F11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11902
dbSNP Id: rs121965070

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280065A>T , CM000666.2:g.186280065A>T GRCh38
NC_000004.11:g.187201219A>T , CM000666.1:g.187201219A>T GRCh37
NC_000004.10:g.187438213A>T NCBI36
NG_008051.1:g.19102A>T , LRG_583:g.19102A>T

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.809A>T , LRG_583t1:c.809A>T NP_000119.1:p.Lys270Ile
XM_005262821.2:c.809A>T XP_005262878.1:p.Lys270Ile
XM_005262822.2:c.809A>T XP_005262879.1:p.Lys270Ile
XM_005262823.2:c.539A>T XP_005262880.1:p.Lys180Ile
XM_005262824.1:c.809A>T XP_005262881.1:p.Lys270Ile
XM_006714137.1:c.809A>T XP_006714200.1:p.Lys270Ile
XR_938706.1:n.1161A>T
XR_938707.1:n.1161A>T
XM_005262821.4:c.809A>T XP_005262878.1:p.Lys270Ile
XM_005262822.4:c.809A>T XP_005262879.1:p.Lys270Ile
XM_005262823.4:c.539A>T XP_005262880.1:p.Lys180Ile
XM_006714137.3:c.809A>T XP_006714200.1:p.Lys270Ile
XM_017007884.2:c.809A>T XP_016863373.1:p.Lys270Ile
XM_017007885.2:c.809A>T XP_016863374.1:p.Lys270Ile
XM_017007886.2:c.809A>T XP_016863375.1:p.Lys270Ile
XR_001741172.2:n.1142A>T
NM_000128.4:c.809A>T VV MANE Preferred NP_000119.1:p.Lys270Ile
ENST00000264692.8:c.647A>T ENSP00000264692.5:p.Lys216Ile
ENST00000403665.6:c.809A>T ENSP00000384957.2:p.Lys270Ile
ENST00000452239.1:n.256A>T