Canonical Allele Identifier: CA363785696
Gene: LHFPL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35782321A>G (hg19) chr6:g.35814544A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814544A>G , CM000668.2:g.35814544A>G GRCh38
NC_000006.11:g.35782321A>G , CM000668.1:g.35782321A>G GRCh37
NC_000006.10:g.35890299A>G NCBI36
NG_012184.1:g.14251A>G
NG_012184.2:g.14251A>G
NG_012184.3:g.22339A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360215.3:c.413-2A>G MANE Select ENSP00000353346.1:n.413-2A>G
ENST00000496656.2:n.192-2A>G
ENST00000651132.1:c.413-2A>G ENSP00000498322.1:n.413-2A>G
ENST00000651676.1:c.413-2A>G ENSP00000498699.1:n.413-2A>G
ENST00000651994.1:c.*70-4893A>G ENSP00000498310.1:n.*70-4893A>G
ENST00000652718.1:c.245-2A>G ENSP00000498866.1:n.245-2A>G
ENST00000360215.2:c.413-2A>G ENSP00000353346.1:n.413-2A>G
ENST00000496656.1:n.192-2A>G
NM_182548.3:c.413-2A>G NP_872354.1:n.413-2A>G
XM_011514403.1:c.413-2A>G XP_011512705.1:n.413-2A>G
NM_182548.4:c.413-2A>G MANE Select NP_872354.1:n.413-2A>G
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