Canonical Allele Identifier: CA1087852152
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs1768922010
gnomAD v3: 6-35823732-T-C
gnomAD v4: 6-35823732-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823732T>C , CM000668.2:g.35823732T>C GRCh38
NC_000006.11:g.35791509T>C , CM000668.1:g.35791509T>C GRCh37
NC_000006.10:g.35899487T>C NCBI36
NG_012184.1:g.23439T>C
NG_012184.2:g.23439T>C
NG_012184.3:g.31527T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*767T>C MANE Select ENSP00000353346.1:n.*767T>C
ENST00000496656.2:n.578+3912T>C
ENST00000651132.1:c.*767T>C ENSP00000498322.1:n.*767T>C
ENST00000651676.1:c.*16+4269T>C ENSP00000498699.1:n.*16+4269T>C
ENST00000651994.1:c.*847T>C ENSP00000498310.1:n.*847T>C
ENST00000652718.1:c.508+4269T>C ENSP00000498866.1:n.508+4269T>C
ENST00000360215.2:c.*767T>C ENSP00000353346.1:n.*767T>C
ENST00000496656.1:n.812+3912T>C
NM_182548.3:c.*767T>C NP_872354.1:n.*767T>C
NM_182548.4:c.*767T>C MANE Select NP_872354.1:n.*767T>C