Canonical Allele Identifier: CA566703537

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1283578316
• gnomAD v2: 6-35782623-A-C
• gnomAD v3: 6-35814846-A-C
• gnomAD v4: 6-35814846-A-C
• MyVariant Identifiers: chr6:g.35782623A>C (hg19) ; chr6:g.35814846A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814846A>C , CM000668.2:g.35814846A>C	GRCh38
NC_000006.11:g.35782623A>C , CM000668.1:g.35782623A>C	GRCh37
NC_000006.10:g.35890601A>C	NCBI36
NG_012184.1:g.14553A>C
NG_012184.2:g.14553A>C
NG_012184.3:g.22641A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.649+64A>C MANE Select	ENSP00000353346.1:n.649+64A>C
ENST00000496656.2:n.428+64A>C
ENST00000651132.1:c.649+64A>C	ENSP00000498322.1:n.649+64A>C
ENST00000651676.1:c.649+64A>C	ENSP00000498699.1:n.649+64A>C
ENST00000651994.1:c.*70-4591A>C	ENSP00000498310.1:n.*70-4591A>C
ENST00000652718.1:c.481+64A>C	ENSP00000498866.1:n.481+64A>C
ENST00000360215.2:c.649+64A>C	ENSP00000353346.1:n.649+64A>C
ENST00000496656.1:n.428+64A>C
NM_182548.3:c.649+64A>C	NP_872354.1:n.649+64A>C
XM_011514403.1:c.649+64A>C	XP_011512705.1:n.649+64A>C
NM_182548.4:c.649+64A>C MANE Select	NP_872354.1:n.649+64A>C