Canonical Allele Identifier: CA566495736
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs1273070328
gnomAD v2: 6-35791181-CACACACACACACACACACACATACATACACACACACATATATAT-C
gnomAD v3: 6-35823404-CACACACACACACACACACACATACATACACACACACATATATAT-C
gnomAD v4: 6-35823404-CACACACACACACACACACACATACATACACACACACATATATAT-C
MyVariant Identifiers: chr6:g.35791182_35791225del (hg19) chr6:g.35823405_35823448del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823426_35823469del , CM000668.2:g.35823426_35823469del GRCh38
NC_000006.11:g.35791203_35791246del , CM000668.1:g.35791203_35791246del GRCh37
NC_000006.10:g.35899181_35899224del NCBI36
NG_012184.1:g.23133_23176del
NG_012184.2:g.23133_23176del
NG_012184.3:g.31221_31264del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*461_*504del MANE Select ENSP00000353346.1:n.*461_*504del
ENST00000496656.2:n.578+3606_578+3649del
ENST00000651132.1:c.*461_*504del ENSP00000498322.1:n.*461_*504del
ENST00000651676.1:c.*16+3963_*16+4006del ENSP00000498699.1:n.*16+3963_*16+4006del
ENST00000651994.1:c.*541_*584del ENSP00000498310.1:n.*541_*584del
ENST00000652718.1:c.508+3963_508+4006del ENSP00000498866.1:n.508+3963_508+4006del
ENST00000360215.2:c.*461_*504del ENSP00000353346.1:n.*461_*504del
ENST00000496656.1:n.812+3606_812+3649del
NM_182548.3:c.*461_*504del NP_872354.1:n.*461_*504del
NM_182548.4:c.*461_*504del MANE Select NP_872354.1:n.*461_*504del
Search 100 bp 5'
Search 100 bp 3'