Canonical Allele Identifier: CA1621068608

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1768903873

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823386_35823397del , CM000668.2:g.35823386_35823397del	GRCh38
NC_000006.11:g.35791163_35791174del , CM000668.1:g.35791163_35791174del	GRCh37
NC_000006.10:g.35899141_35899152del	NCBI36
NG_012184.1:g.23093_23104del
NG_012184.2:g.23093_23104del
NG_012184.3:g.31181_31192del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*421_*432del MANE Select	ENSP00000353346.1:n.*421_*432del
ENST00000496656.2:n.578+3566_578+3577del
ENST00000651132.1:c.*421_*432del	ENSP00000498322.1:n.*421_*432del
ENST00000651676.1:c.*16+3923_*16+3934del	ENSP00000498699.1:n.*16+3923_*16+3934del
ENST00000651994.1:c.*501_*512del	ENSP00000498310.1:n.*501_*512del
ENST00000652718.1:c.508+3923_508+3934del	ENSP00000498866.1:n.508+3923_508+3934del
ENST00000360215.2:c.*421_*432del	ENSP00000353346.1:n.*421_*432del
ENST00000496656.1:n.812+3566_812+3577del
NM_182548.3:c.*421_*432del	NP_872354.1:n.*421_*432del
NM_182548.4:c.*421_*432del MANE Select	NP_872354.1:n.*421_*432del