Canonical Allele Identifier: CA1621068810

Gene: LHFPL5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823524_35823525delinsAG , CM000668.2:g.35823524_35823525delinsAG	GRCh38
NC_000006.11:g.35791301_35791302delinsAG , CM000668.1:g.35791301_35791302delinsAG	GRCh37
NC_000006.10:g.35899279_35899280delinsAG	NCBI36
NG_012184.1:g.23231_23232delinsAG
NG_012184.2:g.23231_23232delinsAG
NG_012184.3:g.31319_31320delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*559_*560delinsAG MANE Select	ENSP00000353346.1:n.*559_*560delinsAG
ENST00000496656.2:n.578+3704_578+3705delinsAG
ENST00000651132.1:c.*559_*560delinsAG	ENSP00000498322.1:n.*559_*560delinsAG
ENST00000651676.1:c.*16+4061_*16+4062delinsAG	ENSP00000498699.1:n.*16+4061_*16+4062delinsAG
ENST00000651994.1:c.*639_*640delinsAG	ENSP00000498310.1:n.*639_*640delinsAG
ENST00000652718.1:c.508+4061_508+4062delinsAG	ENSP00000498866.1:n.508+4061_508+4062delinsAG
ENST00000360215.2:c.*559_*560delinsAG	ENSP00000353346.1:n.*559_*560delinsAG
ENST00000496656.1:n.812+3704_812+3705delinsAG
NM_182548.3:c.*559_*560delinsAG	NP_872354.1:n.*559_*560delinsAG
NM_182548.4:c.*559_*560delinsAG MANE Select	NP_872354.1:n.*559_*560delinsAG