Canonical Allele Identifier: CA566495809

Gene: LHFPL5

Linked Data

• gnomAD v2: 6-35791247-C-CAG
• MyVariant Identifiers: chr6:g.35791247_35791248insAG (hg19) ; chr6:g.35823470_35823471insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823471_35823472insGA , CM000668.2:g.35823471_35823472insGA	GRCh38
NC_000006.11:g.35791248_35791249insGA , CM000668.1:g.35791248_35791249insGA	GRCh37
NC_000006.10:g.35899226_35899227insGA	NCBI36
NG_012184.1:g.23178_23179insGA
NG_012184.2:g.23178_23179insGA
NG_012184.3:g.31266_31267insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*506_*507insGA MANE Select	ENSP00000353346.1:n.*506_*507insGA
ENST00000496656.2:n.578+3651_578+3652insGA
ENST00000651132.1:c.*506_*507insGA	ENSP00000498322.1:n.*506_*507insGA
ENST00000651676.1:c.*16+4008_*16+4009insGA	ENSP00000498699.1:n.*16+4008_*16+4009insGA
ENST00000651994.1:c.*586_*587insGA	ENSP00000498310.1:n.*586_*587insGA
ENST00000652718.1:c.508+4008_508+4009insGA	ENSP00000498866.1:n.508+4008_508+4009insGA
ENST00000360215.2:c.*506_*507insGA	ENSP00000353346.1:n.*506_*507insGA
ENST00000496656.1:n.812+3651_812+3652insGA
NM_182548.3:c.*506_*507insGA	NP_872354.1:n.*506_*507insGA
NM_182548.4:c.*506_*507insGA MANE Select	NP_872354.1:n.*506_*507insGA