Canonical Allele Identifier: CA1621062574

Gene: LHFPL5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35805836_35805885delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT , CM000668.2:g.35805836_35805885delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT	GRCh38
NC_000006.11:g.35773613_35773662delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT , CM000668.1:g.35773613_35773662delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT	GRCh37
NC_000006.10:g.35881591_35881640delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT	NCBI36
NG_012184.1:g.5543_5592delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT
NG_012184.2:g.5543_5592delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT
NG_012184.3:g.13631_13680delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.166_215delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT MANE Select	ENSP00000353346.1:p.Thr56=
ENST00000651132.1:c.166_215delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT	ENSP00000498322.1:p.Thr56=
ENST00000651676.1:c.166_215delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT	ENSP00000498699.1:p.Thr56=
ENST00000651994.1:c.166_215delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT	ENSP00000498310.1:p.Thr56=
ENST00000360215.2:c.166_215delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT	ENSP00000353346.1:p.Thr56=
NM_182548.3:c.166_215delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT	NP_872354.1:p.Thr56=
XM_011514403.1:c.166_215delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT	XP_011512705.1:p.Thr56=
NM_182548.4:c.166_215delinsACACCGCAGGCAGGCTACTTCGGCCTTTTCTCCTACTGCGTGGGTAACGT MANE Select	NP_872354.1:p.Thr56=