Canonical Allele Identifier: CA15433018
Gene: FHL5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96617336G>A , CM000668.2:g.96617336G>A GRCh38
NC_000006.11:g.97065212G>A , CM000668.1:g.97065212G>A GRCh37
NC_000006.10:g.97171933G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000450218.6:c.*1564G>A MANE Select ENSP00000396390.2:n.*1564G>A
XM_006715613.2:c.*1564G>A XP_006715676.1:n.*1564G>A
NM_001170807.2:c.*1564G>A NP_001164278.1:n.*1564G>A
NM_001322466.1:c.*1564G>A NP_001309395.1:n.*1564G>A
NM_001322467.1:c.*1564G>A NP_001309396.1:n.*1564G>A
NM_020482.5:c.*1564G>A NP_065228.4:n.*1564G>A
NM_001170807.3:c.*1564G>A NP_001164278.1:n.*1564G>A
NM_001322466.2:c.*1564G>A MANE Select NP_001309395.1:n.*1564G>A
NM_020482.6:c.*1564G>A NP_065228.4:n.*1564G>A
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