Canonical Allele Identifier: CA363786031

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1435680484
• gnomAD v2: 6-35782442-G-A
• gnomAD v3: 6-35814665-G-A
• gnomAD v4: 6-35814665-G-A
• MyVariant Identifiers: chr6:g.35782442G>A (hg19) ; chr6:g.35814665G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814665G>A , CM000668.2:g.35814665G>A	GRCh38
NC_000006.11:g.35782442G>A , CM000668.1:g.35782442G>A	GRCh37
NC_000006.10:g.35890420G>A	NCBI36
NG_012184.1:g.14372G>A
NG_012184.2:g.14372G>A
NG_012184.3:g.22460G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.532G>A MANE Select	ENSP00000353346.1:p.Ala178Thr
ENST00000496656.2:n.311G>A
ENST00000651132.1:c.532G>A	ENSP00000498322.1:p.Ala178Thr
ENST00000651676.1:c.532G>A	ENSP00000498699.1:p.Ala178Thr
ENST00000651994.1:c.*70-4772G>A	ENSP00000498310.1:n.*70-4772G>A
ENST00000652718.1:c.364G>A	ENSP00000498866.1:p.Ala122Thr
ENST00000360215.2:c.532G>A	ENSP00000353346.1:p.Ala178Thr
ENST00000496656.1:n.311G>A
NM_182548.3:c.532G>A	NP_872354.1:p.Ala178Thr
XM_011514403.1:c.532G>A	XP_011512705.1:p.Ala178Thr
NM_182548.4:c.532G>A MANE Select	NP_872354.1:p.Ala178Thr