Canonical Allele Identifier: CA1621066387
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs1581972093

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814527A>C , CM000668.2:g.35814527A>C GRCh38
NC_000006.11:g.35782304A>C , CM000668.1:g.35782304A>C GRCh37
NC_000006.10:g.35890282A>C NCBI36
NG_012184.1:g.14234A>C
NG_012184.2:g.14234A>C
NG_012184.3:g.22322A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360215.3:c.413-19A>C MANE Select ENSP00000353346.1:n.413-19A>C
ENST00000496656.2:n.192-19A>C
ENST00000651132.1:c.413-19A>C ENSP00000498322.1:n.413-19A>C
ENST00000651676.1:c.413-19A>C ENSP00000498699.1:n.413-19A>C
ENST00000651994.1:c.*70-4910A>C ENSP00000498310.1:n.*70-4910A>C
ENST00000652718.1:c.245-19A>C ENSP00000498866.1:n.245-19A>C
ENST00000360215.2:c.413-19A>C ENSP00000353346.1:n.413-19A>C
ENST00000496656.1:n.192-19A>C
NM_182548.3:c.413-19A>C NP_872354.1:n.413-19A>C
XM_011514403.1:c.413-19A>C XP_011512705.1:n.413-19A>C
NM_182548.4:c.413-19A>C MANE Select NP_872354.1:n.413-19A>C