Canonical Allele Identifier: CA824259379

Gene: LHFPL5

Linked Data

• MyVariant Identifiers: chr6:g.35791226_35791227insAC (hg19) ; chr6:g.35823449_35823450insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823449_35823450insAC , CM000668.2:g.35823449_35823450insAC	GRCh38
NC_000006.11:g.35791226_35791227insAC , CM000668.1:g.35791226_35791227insAC	GRCh37
NC_000006.10:g.35899204_35899205insAC	NCBI36
NG_012184.1:g.23156_23157insAC
NG_012184.2:g.23156_23157insAC
NG_012184.3:g.31244_31245insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*484_*485insAC MANE Select	ENSP00000353346.1:n.*484_*485insAC
ENST00000496656.2:n.578+3629_578+3630insAC
ENST00000651132.1:c.*484_*485insAC	ENSP00000498322.1:n.*484_*485insAC
ENST00000651676.1:c.*16+3986_*16+3987insAC	ENSP00000498699.1:n.*16+3986_*16+3987insAC
ENST00000651994.1:c.*564_*565insAC	ENSP00000498310.1:n.*564_*565insAC
ENST00000652718.1:c.508+3986_508+3987insAC	ENSP00000498866.1:n.508+3986_508+3987insAC
ENST00000360215.2:c.*484_*485insAC	ENSP00000353346.1:n.*484_*485insAC
ENST00000496656.1:n.812+3629_812+3630insAC
NM_182548.3:c.*484_*485insAC	NP_872354.1:n.*484_*485insAC
NM_182548.4:c.*484_*485insAC MANE Select	NP_872354.1:n.*484_*485insAC