Canonical Allele Identifier: CA1087852091

Gene: LHFPL5

Linked Data

• dbSNP Id: rs886061361
• gnomAD v3: 6-35823469-A-ACTCTCTCT
• gnomAD v4: 6-35823469-A-ACTCTCTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823470_35823471insTCTCTCTC , CM000668.2:g.35823470_35823471insTCTCTCTC	GRCh38
NC_000006.11:g.35791247_35791248insTCTCTCTC , CM000668.1:g.35791247_35791248insTCTCTCTC	GRCh37
NC_000006.10:g.35899225_35899226insTCTCTCTC	NCBI36
NG_012184.1:g.23177_23178insTCTCTCTC
NG_012184.2:g.23177_23178insTCTCTCTC
NG_012184.3:g.31265_31266insTCTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*505_*506insTCTCTCTC MANE Select	ENSP00000353346.1:n.*505_*506insTCTCTCTC
ENST00000496656.2:n.578+3650_578+3651insTCTCTCTC
ENST00000651132.1:c.*505_*506insTCTCTCTC	ENSP00000498322.1:n.*505_*506insTCTCTCTC
ENST00000651676.1:c.*16+4007_*16+4008insTCTCTCTC	ENSP00000498699.1:n.*16+4007_*16+4008insTCTCTCTC
ENST00000651994.1:c.*585_*586insTCTCTCTC	ENSP00000498310.1:n.*585_*586insTCTCTCTC
ENST00000652718.1:c.508+4007_508+4008insTCTCTCTC	ENSP00000498866.1:n.508+4007_508+4008insTCTCTCTC
ENST00000360215.2:c.*505_*506insTCTCTCTC	ENSP00000353346.1:n.*505_*506insTCTCTCTC
ENST00000496656.1:n.812+3650_812+3651insTCTCTCTC
NM_182548.3:c.*505_*506insTCTCTCTC	NP_872354.1:n.*505_*506insTCTCTCTC
NM_182548.4:c.*505_*506insTCTCTCTC MANE Select	NP_872354.1:n.*505_*506insTCTCTCTC