Canonical Allele Identifier: CA137313987
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs997921746
MyVariant Identifiers: chr6:g.35791666A>C (hg19) chr6:g.35823889A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823889A>C , CM000668.2:g.35823889A>C GRCh38
NC_000006.11:g.35791666A>C , CM000668.1:g.35791666A>C GRCh37
NC_000006.10:g.35899644A>C NCBI36
NG_012184.1:g.23596A>C
NG_012184.2:g.23596A>C
NG_012184.3:g.31684A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*924A>C MANE Select ENSP00000353346.1:n.*924A>C
ENST00000496656.2:n.578+4069A>C
ENST00000651132.1:c.*924A>C ENSP00000498322.1:n.*924A>C
ENST00000651676.1:c.*16+4426A>C ENSP00000498699.1:n.*16+4426A>C
ENST00000652718.1:c.508+4426A>C ENSP00000498866.1:n.508+4426A>C
ENST00000360215.2:c.*924A>C ENSP00000353346.1:n.*924A>C
ENST00000496656.1:n.812+4069A>C
NM_182548.3:c.*924A>C NP_872354.1:n.*924A>C
NM_182548.4:c.*924A>C MANE Select NP_872354.1:n.*924A>C
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