LDH info

Canonical Allele Identifier: CA31618534
Gene: NOS1AP HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1415259

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115519C>T , CM000663.2:g.162115519C>T GRCh38
NC_000001.10:g.162085309C>T , CM000663.1:g.162085309C>T GRCh37
NC_000001.9:g.160351933C>T NCBI36
NG_015979.1:g.50729C>T
NG_015979.2:g.50729C>T

Transcript Alleles

HGVS Amino-acid change
NM_001164757.1:c.106-38886C>T VV NP_001158229.1:p.=
NM_014697.2:c.106-38886C>T VV NP_055512.1:p.=
XR_922217.1:n.884-1617G>A
XR_922219.1:n.713-1617G>A
XR_922221.1:n.713-8771G>A
XR_002958375.1:n.3842-1617G>A
XR_002958378.1:n.3671-1617G>A
NM_014697.3:c.106-38886C>T VV MANE Preferred NP_055512.1:p.=
ENST00000361897.9:c.106-38886C>T ENSP00000355133.5:p.=
ENST00000430120.3:c.106-38886C>T ENSP00000396713.3:p.=
ENST00000530878.5:c.106-38886C>T ENSP00000431586.1:p.=