Canonical Allele Identifier: CA363785932

Gene: LHFPL5

Linked Data

• MyVariant Identifiers: chr6:g.35782415A>G (hg19) ; chr6:g.35814638A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814638A>G , CM000668.2:g.35814638A>G	GRCh38
NC_000006.11:g.35782415A>G , CM000668.1:g.35782415A>G	GRCh37
NC_000006.10:g.35890393A>G	NCBI36
NG_012184.1:g.14345A>G
NG_012184.2:g.14345A>G
NG_012184.3:g.22433A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.505A>G MANE Select	ENSP00000353346.1:p.Thr169Ala
ENST00000496656.2:n.284A>G
ENST00000651132.1:c.505A>G	ENSP00000498322.1:p.Thr169Ala
ENST00000651676.1:c.505A>G	ENSP00000498699.1:p.Thr169Ala
ENST00000651994.1:c.*70-4799A>G	ENSP00000498310.1:n.*70-4799A>G
ENST00000652718.1:c.337A>G	ENSP00000498866.1:p.Thr113Ala
ENST00000360215.2:c.505A>G	ENSP00000353346.1:p.Thr169Ala
ENST00000496656.1:n.284A>G
NM_182548.3:c.505A>G	NP_872354.1:p.Thr169Ala
XM_011514403.1:c.505A>G	XP_011512705.1:p.Thr169Ala
NM_182548.4:c.505A>G MANE Select	NP_872354.1:p.Thr169Ala