Canonical Allele Identifier: CA824259619

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1554147856
• gnomAD v3: 6-35823477-A-ACACTCTCT
• gnomAD v4: 6-35823477-A-ACACTCTCT
• MyVariant Identifiers: chr6:g.35791254_35791255insCACTCTCT (hg19) ; chr6:g.35823477_35823478insCACTCTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823478_35823479insACTCTCTC , CM000668.2:g.35823478_35823479insACTCTCTC	GRCh38
NC_000006.11:g.35791255_35791256insACTCTCTC , CM000668.1:g.35791255_35791256insACTCTCTC	GRCh37
NC_000006.10:g.35899233_35899234insACTCTCTC	NCBI36
NG_012184.1:g.23185_23186insACTCTCTC
NG_012184.2:g.23185_23186insACTCTCTC
NG_012184.3:g.31273_31274insACTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*513_*514insACTCTCTC MANE Select	ENSP00000353346.1:n.*513_*514insACTCTCTC
ENST00000496656.2:n.578+3658_578+3659insACTCTCTC
ENST00000651132.1:c.*513_*514insACTCTCTC	ENSP00000498322.1:n.*513_*514insACTCTCTC
ENST00000651676.1:c.*16+4015_*16+4016insACTCTCTC	ENSP00000498699.1:n.*16+4015_*16+4016insACTCTCTC
ENST00000651994.1:c.*593_*594insACTCTCTC	ENSP00000498310.1:n.*593_*594insACTCTCTC
ENST00000652718.1:c.508+4015_508+4016insACTCTCTC	ENSP00000498866.1:n.508+4015_508+4016insACTCTCTC
ENST00000360215.2:c.*513_*514insACTCTCTC	ENSP00000353346.1:n.*513_*514insACTCTCTC
ENST00000496656.1:n.812+3658_812+3659insACTCTCTC
NM_182548.3:c.*513_*514insACTCTCTC	NP_872354.1:n.*513_*514insACTCTCTC
NM_182548.4:c.*513_*514insACTCTCTC MANE Select	NP_872354.1:n.*513_*514insACTCTCTC