Canonical Allele Identifier: CA363785203

Gene: LHFPL5

Linked Data

• gnomAD v4: 6-35806062-C-G
• MyVariant Identifiers: chr6:g.35773839C>G (hg19) ; chr6:g.35806062C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35806062C>G , CM000668.2:g.35806062C>G	GRCh38
NC_000006.11:g.35773839C>G , CM000668.1:g.35773839C>G	GRCh37
NC_000006.10:g.35881817C>G	NCBI36
NG_012184.1:g.5769C>G
NG_012184.2:g.5769C>G
NG_012184.3:g.13857C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.392C>G MANE Select	ENSP00000353346.1:p.Ala131Gly
ENST00000651132.1:c.392C>G	ENSP00000498322.1:p.Ala131Gly
ENST00000651676.1:c.392C>G	ENSP00000498699.1:p.Ala131Gly
ENST00000651994.1:c.392C>G	ENSP00000498310.1:p.Ala131Gly
ENST00000652718.1:c.224C>G	ENSP00000498866.1:p.Ala75Gly
ENST00000360215.2:c.392C>G	ENSP00000353346.1:p.Ala131Gly
NM_182548.3:c.392C>G	NP_872354.1:p.Ala131Gly
XM_011514403.1:c.392C>G	XP_011512705.1:p.Ala131Gly
NM_182548.4:c.392C>G MANE Select	NP_872354.1:p.Ala131Gly