Canonical Allele Identifier: CA566495631

Gene: LHFPL5

Linked Data

• gnomAD v2: 6-35791144-G-GCATACACACACACATATATATACACACACACACACACACACACA
• gnomAD v3: 6-35823367-G-GCATACACACACACATATATATACACACACACACACACACACACA
• gnomAD v4: 6-35823367-G-GCATACACACACACATATATATACACACACACACACACACACACA
• MyVariant Identifiers: chr6:g.35791191_35791204delinsTACACACACACATATATATACACACACACACACACACACACACACACACACACACATA (hg19) ; chr6:g.35823414_35823427delinsTACACACACACATATATATACACACACACACACACACACACACACACACACACACATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823370_35823413dup , CM000668.2:g.35823370_35823413dup	GRCh38
NC_000006.11:g.35791147_35791190dup , CM000668.1:g.35791147_35791190dup	GRCh37
NC_000006.10:g.35899125_35899168dup	NCBI36
NG_012184.1:g.23077_23120dup
NG_012184.2:g.23077_23120dup
NG_012184.3:g.31165_31208dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*405_*448dup MANE Select	ENSP00000353346.1:n.*405_*448dup
ENST00000496656.2:n.578+3550_578+3593dup
ENST00000651132.1:c.*405_*448dup	ENSP00000498322.1:n.*405_*448dup
ENST00000651676.1:c.*16+3907_*16+3950dup	ENSP00000498699.1:n.*16+3907_*16+3950dup
ENST00000651994.1:c.*485_*528dup	ENSP00000498310.1:n.*485_*528dup
ENST00000652718.1:c.508+3907_508+3950dup	ENSP00000498866.1:n.508+3907_508+3950dup
ENST00000360215.2:c.*405_*448dup	ENSP00000353346.1:n.*405_*448dup
ENST00000496656.1:n.812+3550_812+3593dup
NM_182548.3:c.*405_*448dup	NP_872354.1:n.*405_*448dup
NM_182548.4:c.*405_*448dup MANE Select	NP_872354.1:n.*405_*448dup