Canonical Allele Identifier: CA1087852089

Gene: LHFPL5

Linked Data

• gnomAD v3: 6-35823467-A-ACCCTCT
• gnomAD v4: 6-35823467-A-ACCCTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823468_35823469insCCTCTC , CM000668.2:g.35823468_35823469insCCTCTC	GRCh38
NC_000006.11:g.35791245_35791246insCCTCTC , CM000668.1:g.35791245_35791246insCCTCTC	GRCh37
NC_000006.10:g.35899223_35899224insCCTCTC	NCBI36
NG_012184.1:g.23175_23176insCCTCTC
NG_012184.2:g.23175_23176insCCTCTC
NG_012184.3:g.31263_31264insCCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*503_*504insCCTCTC MANE Select	ENSP00000353346.1:n.*503_*504insCCTCTC
ENST00000496656.2:n.578+3648_578+3649insCCTCTC
ENST00000651132.1:c.*503_*504insCCTCTC	ENSP00000498322.1:n.*503_*504insCCTCTC
ENST00000651676.1:c.*16+4005_*16+4006insCCTCTC	ENSP00000498699.1:n.*16+4005_*16+4006insCCTCTC
ENST00000651994.1:c.*583_*584insCCTCTC	ENSP00000498310.1:n.*583_*584insCCTCTC
ENST00000652718.1:c.508+4005_508+4006insCCTCTC	ENSP00000498866.1:n.508+4005_508+4006insCCTCTC
ENST00000360215.2:c.*503_*504insCCTCTC	ENSP00000353346.1:n.*503_*504insCCTCTC
ENST00000496656.1:n.812+3648_812+3649insCCTCTC
NM_182548.3:c.*503_*504insCCTCTC	NP_872354.1:n.*503_*504insCCTCTC
NM_182548.4:c.*503_*504insCCTCTC MANE Select	NP_872354.1:n.*503_*504insCCTCTC