LDH info

Canonical Allele Identifier: CA11915819
Gene: CLPTM1L HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs401681

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1321972C>T , CM000667.2:g.1321972C>T GRCh38
NC_000005.9:g.1322087C>T , CM000667.1:g.1322087C>T GRCh37
NC_000005.8:g.1375087C>T NCBI36
NG_046903.1:g.28094G>A

Transcript Alleles

HGVS Amino-acid change
NM_030782.3:c.1316-153G>A VV NP_110409.2:p.=
NM_030782.4:c.1316-153G>A VV NP_110409.2:p.=
XM_011514144.1:c.1313-153G>A XP_011512446.1:p.=
XM_011514144.2:c.1313-153G>A XP_011512446.1:p.=
XM_024446221.1:c.1316-153G>A XP_024301989.1:p.=
XM_024446222.1:c.782-153G>A XP_024301990.1:p.=
XR_002956182.1:n.1359-153G>A
XR_002956183.1:n.1537-153G>A
NM_030782.5:c.1316-153G>A VV MANE Preferred NP_110409.2:p.=
ENST00000320895.9:c.1316-153G>A ENSP00000313854.5:p.=
ENST00000503042.5:n.2738-153G>A
ENST00000503534.5:n.247-153G>A
ENST00000505605.5:n.214-153G>A
ENST00000505914.5:n.287-153G>A
ENST00000506641.5:n.477-153G>A
ENST00000507195.5:n.412-153G>A
ENST00000507807.3:c.809-153G>A ENSP00000423321.1:p.=
ENST00000511268.6:n.80-153G>A
ENST00000512451.5:n.40-153G>A
ENST00000630539.1:c.809-153G>A ENSP00000485923.1:p.=