Canonical Allele Identifier: CA1621068626
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs67626900

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823404_35823425del , CM000668.2:g.35823404_35823425del GRCh38
NC_000006.11:g.35791181_35791202del , CM000668.1:g.35791181_35791202del GRCh37
NC_000006.10:g.35899159_35899180del NCBI36
NG_012184.1:g.23111_23132del
NG_012184.2:g.23111_23132del
NG_012184.3:g.31199_31220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*439_*460del MANE Select ENSP00000353346.1:n.*439_*460del
ENST00000496656.2:n.578+3584_578+3605del
ENST00000651132.1:c.*439_*460del ENSP00000498322.1:n.*439_*460del
ENST00000651676.1:c.*16+3941_*16+3962del ENSP00000498699.1:n.*16+3941_*16+3962del
ENST00000651994.1:c.*519_*540del ENSP00000498310.1:n.*519_*540del
ENST00000652718.1:c.508+3941_508+3962del ENSP00000498866.1:n.508+3941_508+3962del
ENST00000360215.2:c.*439_*460del ENSP00000353346.1:n.*439_*460del
ENST00000496656.1:n.812+3584_812+3605del
NM_182548.3:c.*439_*460del NP_872354.1:n.*439_*460del
NM_182548.4:c.*439_*460del MANE Select NP_872354.1:n.*439_*460del