Canonical Allele Identifier: CA363786399

Gene: LHFPL5

Linked Data

• MyVariant Identifiers: chr6:g.35782541T>G (hg19) ; chr6:g.35814764T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814764T>G , CM000668.2:g.35814764T>G	GRCh38
NC_000006.11:g.35782541T>G , CM000668.1:g.35782541T>G	GRCh37
NC_000006.10:g.35890519T>G	NCBI36
NG_012184.1:g.14471T>G
NG_012184.2:g.14471T>G
NG_012184.3:g.22559T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.631T>G MANE Select	ENSP00000353346.1:p.Tyr211Asp
ENST00000496656.2:n.410T>G
ENST00000651132.1:c.631T>G	ENSP00000498322.1:p.Tyr211Asp
ENST00000651676.1:c.631T>G	ENSP00000498699.1:p.Tyr211Asp
ENST00000651994.1:c.*70-4673T>G	ENSP00000498310.1:n.*70-4673T>G
ENST00000652718.1:c.463T>G	ENSP00000498866.1:p.Tyr155Asp
ENST00000360215.2:c.631T>G	ENSP00000353346.1:p.Tyr211Asp
ENST00000496656.1:n.410T>G
NM_182548.3:c.631T>G	NP_872354.1:p.Tyr211Asp
XM_011514403.1:c.631T>G	XP_011512705.1:p.Tyr211Asp
NM_182548.4:c.631T>G MANE Select	NP_872354.1:p.Tyr211Asp