Canonical Allele Identifier: CA137313847

Gene: LHFPL5

Linked Data

• MyVariant Identifiers: chr6:g.35791254_35791255insAC (hg19) ; chr6:g.35823477_35823478insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823477_35823478insAC , CM000668.2:g.35823477_35823478insAC	GRCh38
NC_000006.11:g.35791254_35791255insAC , CM000668.1:g.35791254_35791255insAC	GRCh37
NC_000006.10:g.35899232_35899233insAC	NCBI36
NG_012184.1:g.23184_23185insAC
NG_012184.2:g.23184_23185insAC
NG_012184.3:g.31272_31273insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*512_*513insAC MANE Select	ENSP00000353346.1:n.*512_*513insAC
ENST00000496656.2:n.578+3657_578+3658insAC
ENST00000651132.1:c.*512_*513insAC	ENSP00000498322.1:n.*512_*513insAC
ENST00000651676.1:c.*16+4014_*16+4015insAC	ENSP00000498699.1:n.*16+4014_*16+4015insAC
ENST00000651994.1:c.*592_*593insAC	ENSP00000498310.1:n.*592_*593insAC
ENST00000652718.1:c.508+4014_508+4015insAC	ENSP00000498866.1:n.508+4014_508+4015insAC
ENST00000360215.2:c.*512_*513insAC	ENSP00000353346.1:n.*512_*513insAC
ENST00000496656.1:n.812+3657_812+3658insAC
NM_182548.3:c.*512_*513insAC	NP_872354.1:n.*512_*513insAC
NM_182548.4:c.*512_*513insAC MANE Select	NP_872354.1:n.*512_*513insAC