Canonical Allele Identifier: CA363786035

Gene: LHFPL5

Linked Data

• gnomAD v4: 6-35814665-G-C
• MyVariant Identifiers: chr6:g.35782442G>C (hg19) ; chr6:g.35814665G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.532G>C MANE Select	ENSP00000353346.1:p.Ala178Pro
ENST00000496656.2:n.311G>C
ENST00000651132.1:c.532G>C	ENSP00000498322.1:p.Ala178Pro
ENST00000651676.1:c.532G>C	ENSP00000498699.1:p.Ala178Pro
ENST00000651994.1:c.*70-4772G>C	ENSP00000498310.1:n.*70-4772G>C
ENST00000652718.1:c.364G>C	ENSP00000498866.1:p.Ala122Pro
ENST00000360215.2:c.532G>C	ENSP00000353346.1:p.Ala178Pro
ENST00000496656.1:n.311G>C
NM_182548.3:c.532G>C	NP_872354.1:p.Ala178Pro
XM_011514403.1:c.532G>C	XP_011512705.1:p.Ala178Pro
NM_182548.4:c.532G>C MANE Select	NP_872354.1:p.Ala178Pro