Canonical Allele Identifier: CA1621068864

Gene: LHFPL5

Linked Data

• dbSNP Id: rs972926378

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823633_35823634insA , CM000668.2:g.35823633_35823634insA	GRCh38
NC_000006.11:g.35791410_35791411insA , CM000668.1:g.35791410_35791411insA	GRCh37
NC_000006.10:g.35899388_35899389insA	NCBI36
NG_012184.1:g.23340_23341insA
NG_012184.2:g.23340_23341insA
NG_012184.3:g.31428_31429insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*668_*669insA MANE Select	ENSP00000353346.1:n.*668_*669insA
ENST00000496656.2:n.578+3813_578+3814insA
ENST00000651132.1:c.*668_*669insA	ENSP00000498322.1:n.*668_*669insA
ENST00000651676.1:c.*16+4170_*16+4171insA	ENSP00000498699.1:n.*16+4170_*16+4171insA
ENST00000651994.1:c.*748_*749insA	ENSP00000498310.1:n.*748_*749insA
ENST00000652718.1:c.508+4170_508+4171insA	ENSP00000498866.1:n.508+4170_508+4171insA
ENST00000360215.2:c.*668_*669insA	ENSP00000353346.1:n.*668_*669insA
ENST00000496656.1:n.812+3813_812+3814insA
NM_182548.3:c.*668_*669insA	NP_872354.1:n.*668_*669insA
NM_182548.4:c.*668_*669insA MANE Select	NP_872354.1:n.*668_*669insA