Canonical Allele Identifier: CA1621068952
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs1263755400

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823826T>G , CM000668.2:g.35823826T>G GRCh38
NC_000006.11:g.35791603T>G , CM000668.1:g.35791603T>G GRCh37
NC_000006.10:g.35899581T>G NCBI36
NG_012184.1:g.23533T>G
NG_012184.2:g.23533T>G
NG_012184.3:g.31621T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*861T>G MANE Select ENSP00000353346.1:n.*861T>G
ENST00000496656.2:n.578+4006T>G
ENST00000651132.1:c.*861T>G ENSP00000498322.1:n.*861T>G
ENST00000651676.1:c.*16+4363T>G ENSP00000498699.1:n.*16+4363T>G
ENST00000651994.1:c.*941T>G ENSP00000498310.1:n.*941T>G
ENST00000652718.1:c.508+4363T>G ENSP00000498866.1:n.508+4363T>G
ENST00000360215.2:c.*861T>G ENSP00000353346.1:n.*861T>G
ENST00000496656.1:n.812+4006T>G
NM_182548.3:c.*861T>G NP_872354.1:n.*861T>G
NM_182548.4:c.*861T>G MANE Select NP_872354.1:n.*861T>G