Canonical Allele Identifier: CA566495713
Gene: LHFPL5 HGNC NCBI

Linked Data

gnomAD v2: 6-35791167-CACACACACACACACACACACACACACACACACACATACATACACACACACATATATAT-C
gnomAD v3: 6-35823390-CACACACACACACACACACACACACACACACACACATACATACACACACACATATATAT-C
gnomAD v4: 6-35823390-CACACACACACACACACACACACACACACACACACATACATACACACACACATATATAT-C
MyVariant Identifiers: chr6:g.35791168_35791225del (hg19) chr6:g.35823391_35823448del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823421_35823478del , CM000668.2:g.35823421_35823478del GRCh38
NC_000006.11:g.35791198_35791255del , CM000668.1:g.35791198_35791255del GRCh37
NC_000006.10:g.35899176_35899233del NCBI36
NG_012184.1:g.23128_23185del
NG_012184.2:g.23128_23185del
NG_012184.3:g.31216_31273del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*456_*513del MANE Select ENSP00000353346.1:n.*456_*513del
ENST00000496656.2:n.578+3601_578+3658del
ENST00000651132.1:c.*456_*513del ENSP00000498322.1:n.*456_*513del
ENST00000651676.1:c.*16+3958_*16+4015del ENSP00000498699.1:n.*16+3958_*16+4015del
ENST00000651994.1:c.*536_*593del ENSP00000498310.1:n.*536_*593del
ENST00000652718.1:c.508+3958_508+4015del ENSP00000498866.1:n.508+3958_508+4015del
ENST00000360215.2:c.*456_*513del ENSP00000353346.1:n.*456_*513del
ENST00000496656.1:n.812+3601_812+3658del
NM_182548.3:c.*456_*513del NP_872354.1:n.*456_*513del
NM_182548.4:c.*456_*513del MANE Select NP_872354.1:n.*456_*513del
Search 100 bp 5'
Search 100 bp 3'