LDH info

Canonical Allele Identifier: CA15217728
Gene: TTC7A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17540621

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47002700G>C , CM000664.2:g.47002700G>C GRCh38
NC_000002.11:g.47229839G>C , CM000664.1:g.47229839G>C GRCh37
NC_000002.10:g.47083343G>C NCBI36
NG_034143.1:g.91572G>C
NG_034143.2:g.91572G>C

Transcript Alleles

HGVS Amino-acid change
NM_001288951.1:c.1066-3222G>C VV NP_001275880.1:p.=
NM_001288953.1:c.964-3222G>C VV NP_001275882.1:p.=
NM_001288955.1:c.4-3222G>C VV NP_001275884.1:p.=
NM_020458.3:c.1066-3222G>C VV NP_065191.2:p.=
XM_005264439.2:c.709-3222G>C XP_005264496.1:p.=
XM_011532998.1:c.709-3222G>C XP_011531300.1:p.=
XM_011532999.1:c.1066-3222G>C XP_011531301.1:p.=
XM_011533000.1:c.286-3222G>C XP_011531302.1:p.=
XR_939696.1:n.1371-3222G>C
XM_005264439.4:c.709-3222G>C XP_005264496.1:p.=
XM_011532998.3:c.709-3222G>C XP_011531300.1:p.=
XM_011532999.2:c.1066-3222G>C XP_011531301.1:p.=
XM_011533000.3:c.286-3222G>C XP_011531302.1:p.=
XM_017004524.1:c.1066-3222G>C XP_016860013.1:p.=
XM_017004525.1:c.898-3222G>C XP_016860014.1:p.=
XM_017004526.1:c.1066-3222G>C XP_016860015.1:p.=
XM_017004529.1:c.1066-3222G>C XP_016860018.1:p.=
XM_024453013.1:c.31-3222G>C XP_024308781.1:p.=
XR_001738853.2:n.1378-3222G>C
XR_001738854.1:n.1377-3222G>C
NM_020458.4:c.1066-3222G>C VV NP_065191.2:p.=
ENST00000319190.9:c.1066-3222G>C ENSP00000316699.5:p.=
ENST00000394850.6:c.1066-3222G>C ENSP00000378320.2:p.=
ENST00000409245.5:c.964-3222G>C ENSP00000386307.1:p.=
ENST00000409825.5:n.1014-3222G>C
ENST00000441914.5:n.907-3222G>C
ENST00000461601.5:n.1391-3222G>C
ENST00000474321.6:n.550-3222G>C
ENST00000484061.5:n.349-3222G>C
ENST00000491786.5:n.470-3222G>C