Canonical Allele Identifier: CA363785808

Gene: LHFPL5

Linked Data

• gnomAD v4: 6-35814597-G-C
• MyVariant Identifiers: chr6:g.35782374G>C (hg19) ; chr6:g.35814597G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814597G>C , CM000668.2:g.35814597G>C	GRCh38
NC_000006.11:g.35782374G>C , CM000668.1:g.35782374G>C	GRCh37
NC_000006.10:g.35890352G>C	NCBI36
NG_012184.1:g.14304G>C
NG_012184.2:g.14304G>C
NG_012184.3:g.22392G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.464G>C MANE Select	ENSP00000353346.1:p.Ser155Thr
ENST00000496656.2:n.243G>C
ENST00000651132.1:c.464G>C	ENSP00000498322.1:p.Ser155Thr
ENST00000651676.1:c.464G>C	ENSP00000498699.1:p.Ser155Thr
ENST00000651994.1:c.*70-4840G>C	ENSP00000498310.1:n.*70-4840G>C
ENST00000652718.1:c.296G>C	ENSP00000498866.1:p.Ser99Thr
ENST00000360215.2:c.464G>C	ENSP00000353346.1:p.Ser155Thr
ENST00000496656.1:n.243G>C
NM_182548.3:c.464G>C	NP_872354.1:p.Ser155Thr
XM_011514403.1:c.464G>C	XP_011512705.1:p.Ser155Thr
NM_182548.4:c.464G>C MANE Select	NP_872354.1:p.Ser155Thr