Canonical Allele Identifier: CA1087852012

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1768906838
• gnomAD v3: 6-35823408-C-CAT
• gnomAD v4: 6-35823408-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823409_35823410insTA , CM000668.2:g.35823409_35823410insTA	GRCh38
NC_000006.11:g.35791186_35791187insTA , CM000668.1:g.35791186_35791187insTA	GRCh37
NC_000006.10:g.35899164_35899165insTA	NCBI36
NG_012184.1:g.23116_23117insTA
NG_012184.2:g.23116_23117insTA
NG_012184.3:g.31204_31205insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*444_*445insTA MANE Select	ENSP00000353346.1:n.*444_*445insTA
ENST00000496656.2:n.578+3589_578+3590insTA
ENST00000651132.1:c.*444_*445insTA	ENSP00000498322.1:n.*444_*445insTA
ENST00000651676.1:c.*16+3946_*16+3947insTA	ENSP00000498699.1:n.*16+3946_*16+3947insTA
ENST00000651994.1:c.*524_*525insTA	ENSP00000498310.1:n.*524_*525insTA
ENST00000652718.1:c.508+3946_508+3947insTA	ENSP00000498866.1:n.508+3946_508+3947insTA
ENST00000360215.2:c.*444_*445insTA	ENSP00000353346.1:n.*444_*445insTA
ENST00000496656.1:n.812+3589_812+3590insTA
NM_182548.3:c.*444_*445insTA	NP_872354.1:n.*444_*445insTA
NM_182548.4:c.*444_*445insTA MANE Select	NP_872354.1:n.*444_*445insTA