Canonical Allele Identifier: CA824259841

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1459087097
• gnomAD v3: 6-35823808-T-C
• gnomAD v4: 6-35823808-T-C
• MyVariant Identifiers: chr6:g.35791585T>C (hg19) ; chr6:g.35823808T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823808T>C , CM000668.2:g.35823808T>C	GRCh38
NC_000006.11:g.35791585T>C , CM000668.1:g.35791585T>C	GRCh37
NC_000006.10:g.35899563T>C	NCBI36
NG_012184.1:g.23515T>C
NG_012184.2:g.23515T>C
NG_012184.3:g.31603T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*843T>C MANE Select	ENSP00000353346.1:n.*843T>C
ENST00000496656.2:n.578+3988T>C
ENST00000651132.1:c.*843T>C	ENSP00000498322.1:n.*843T>C
ENST00000651676.1:c.*16+4345T>C	ENSP00000498699.1:n.*16+4345T>C
ENST00000651994.1:c.*923T>C	ENSP00000498310.1:n.*923T>C
ENST00000652718.1:c.508+4345T>C	ENSP00000498866.1:n.508+4345T>C
ENST00000360215.2:c.*843T>C	ENSP00000353346.1:n.*843T>C
ENST00000496656.1:n.812+3988T>C
NM_182548.3:c.*843T>C	NP_872354.1:n.*843T>C
NM_182548.4:c.*843T>C MANE Select	NP_872354.1:n.*843T>C