LDH info

Canonical Allele Identifier: CA15367195
Gene: TRIO HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10065203

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14393512C>T , CM000667.2:g.14393512C>T GRCh38
NC_000005.9:g.14393621C>T , CM000667.1:g.14393621C>T GRCh37
NC_000005.8:g.14446621C>T NCBI36
NG_052962.1:g.254811C>T

Transcript Alleles

HGVS Amino-acid change
NM_007118.2:c.4219-526C>T VV NP_009049.2:p.=
XM_011514107.1:c.4156-526C>T XP_011512409.1:p.=
XM_011514108.1:c.4102-526C>T XP_011512410.1:p.=
XM_011514109.1:c.4072-526C>T XP_011512411.1:p.=
XM_011514110.1:c.4042-526C>T XP_011512412.1:p.=
XM_011514111.1:c.4042-526C>T XP_011512413.1:p.=
XM_011514112.1:c.2764-526C>T XP_011512414.1:p.=
XM_011514113.1:c.4219-526C>T XP_011512415.1:p.=
XR_241714.1:n.4237-526C>T
NM_007118.3:c.4219-526C>T VV NP_009049.2:p.=
NR_134469.1:n.4243-526C>T
XM_011514107.2:c.4156-526C>T XP_011512409.1:p.=
XM_011514109.3:c.4072-526C>T XP_011512411.1:p.=
XM_011514110.3:c.4042-526C>T XP_011512412.1:p.=
XM_017009801.1:c.4219-526C>T XP_016865290.1:p.=
XM_017009802.1:c.4219-526C>T XP_016865291.1:p.=
XM_017009803.1:c.2764-526C>T XP_016865292.1:p.=
XR_001742236.2:n.4595-526C>T
NM_007118.4:c.4219-526C>T VV MANE Preferred NP_009049.2:p.=
NR_134469.2:n.4603-526C>T
ENST00000344204.8:c.4219-526C>T ENSP00000339299.4:p.=
ENST00000502490.1:n.407-526C>T
ENST00000509967.6:c.4072-526C>T ENSP00000445592.1:p.=
ENST00000512070.6:c.4042-526C>T ENSP00000421555.2:p.=
ENST00000513206.5:n.3418-526C>T ENSP00000426342.2:p.=
ENST00000515144.5:n.3137-526C>T