LDH info

Canonical Allele Identifier: CA342061
Gene: CRLF1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 21430
ClinVar RCV Id: RCV000020615
dbSNP Id: rs137853931

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599660del , CM000681.2:g.18599660del GRCh38
NC_000019.9:g.18710470del , CM000681.1:g.18710470del GRCh37
NC_000019.8:g.18571470del NCBI36
NG_013370.1:g.12192del

Transcript Alleles

HGVS Amino-acid change
NM_004750.4:c.303del VV NP_004741.1:p.Asn102ThrfsTer?
XM_011528422.1:c.237del XP_011526724.1:p.Asn80ThrfsTer?
XM_011528423.1:n.303del XP_011526725.1:p.Asn102ThrfsTer?
XM_011528424.1:c.237del XP_011526726.1:p.Asn80ThrfsTer?
XM_011528422.2:c.237del XP_011526724.1:p.Asn80ThrfsTer?
XM_011528423.2:n.303del XP_011526725.1:p.Asn102ThrfsTer?
XM_011528424.3:c.237del XP_011526726.1:p.Asn80ThrfsTer?
NM_004750.5:c.303del VV MANE Preferred NP_004741.1:p.Asn102ThrfsTer?
ENST00000392386.7:c.303del ENSP00000376188.2:p.Asn102ThrfsTer?