LDH info

Canonical Allele Identifier: CA5540319
Gene: ADAMTS14 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6480463

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70758081C>T , CM000672.2:g.70758081C>T GRCh38
NC_000010.10:g.72517837C>T , CM000672.1:g.72517837C>T GRCh37
NC_000010.9:g.72187843C>T NCBI36
NG_042147.1:g.90279C>T

Transcript Alleles

HGVS Amino-acid change
NM_080722.3:n.3057C>T VV NP_542453.2:p.Pro1019=
NM_139155.2:n.3066C>T VV NP_631894.2:p.Pro1022=
XM_011539300.1:c.2556C>T XP_011537602.1:p.Pro852=
XM_011539301.1:c.2130C>T XP_011537603.1:p.Pro710=
XM_011539302.1:c.2130C>T XP_011537604.1:p.Pro710=
XM_011539309.1:c.1626C>T XP_011537611.1:p.Pro542=
NM_080722.4:c.3057C>T VV MANE Preferred NP_542453.2:p.Pro1019=
NM_139155.3:c.3066C>T VV NP_631894.2:p.Pro1022=
XM_011539300.2:c.2556C>T XP_011537602.1:p.Pro852=
XM_011539301.2:c.2130C>T XP_011537603.1:p.Pro710=
XM_011539302.2:c.2130C>T XP_011537604.1:p.Pro710=
ENST00000373207.1:n.3057C>T ENSP00000362303.1:p.Pro1019=
ENST00000373208.5:n.3066C>T ENSP00000362304.1:p.Pro1022=