Canonical Allele Identifier: CA824258501

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1403761317
• MyVariant Identifiers: chr6:g.35791110C>G (hg19) ; chr6:g.35823333C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823333C>G , CM000668.2:g.35823333C>G	GRCh38
NC_000006.11:g.35791110C>G , CM000668.1:g.35791110C>G	GRCh37
NC_000006.10:g.35899088C>G	NCBI36
NG_012184.1:g.23040C>G
NG_012184.2:g.23040C>G
NG_012184.3:g.31128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*368C>G MANE Select	ENSP00000353346.1:n.*368C>G
ENST00000496656.2:n.578+3513C>G
ENST00000651132.1:c.*368C>G	ENSP00000498322.1:n.*368C>G
ENST00000651676.1:c.*16+3870C>G	ENSP00000498699.1:n.*16+3870C>G
ENST00000651994.1:c.*448C>G	ENSP00000498310.1:n.*448C>G
ENST00000652718.1:c.508+3870C>G	ENSP00000498866.1:n.508+3870C>G
ENST00000360215.2:c.*368C>G	ENSP00000353346.1:n.*368C>G
ENST00000496656.1:n.812+3513C>G
NM_182548.3:c.*368C>G	NP_872354.1:n.*368C>G
XM_011514403.1:c.*368C>G	XP_011512705.1:n.*368C>G
NM_182548.4:c.*368C>G MANE Select	NP_872354.1:n.*368C>G